NP-MRD: Showing NP-Card for 3,11-dimethylnonacosan-2-one (NP0293988)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-10 02:18:01 UTC

Updated at

2022-09-10 02:18:01 UTC

NP-MRD ID

NP0293988

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3,11-dimethylnonacosan-2-one

Description

3,11-Dimethylnonacosan-2-one belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol. Thus, 3,11-dimethylnonacosan-2-one is considered to be an oxygenated hydrocarbon lipid molecule. 3,11-dimethylnonacosan-2-one is found in Blattella germanica. 3,11-Dimethylnonacosan-2-one is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004151516362D          

 32 31  0  0  0  0            999 V2000
   15.3730    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0875    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8020    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5164    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2309    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9454    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6599    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3743    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0888    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.8033    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.5177    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2322    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9467    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6612    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3756    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0901    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.8046    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.5190    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.2335    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.2335   10.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9480    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.6624    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3769    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.0914    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.8059    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.5203    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.2348    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.9493    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.9493   10.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6637    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3782    9.7006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.6637    8.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END

     RDKit          3D

 94 93  0  0  0  0  0  0  0  0999 V2000
   11.2132   -1.7275    0.1952 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.9348   -1.1334   -0.9814 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0817   -1.3269   -2.2330 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7704   -0.6012   -1.9534 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8321   -0.7192   -3.1247 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5409   -0.0245   -2.8157 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7578    1.4310   -2.5425 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4480    2.1273   -2.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7636    1.5326   -1.0822 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4640    2.3018   -0.8615 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6880    1.7947    0.3278 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3210    0.3607    0.1453 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -0.2099    1.2964 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2510    0.4614    1.5915 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2749    0.4341    0.4667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0207    1.1256    0.8079 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7191    0.4863    1.9885 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0204    1.1976    2.3091 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7258    0.5723    3.4819 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8349    0.6379    4.7029 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1264   -0.8455    3.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0688   -1.0624    2.1204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3366   -0.2805    2.3830 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2617   -0.5549    1.1521 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5089    0.1928    1.3898 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6262    0.0671    0.4702 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5083    0.4530   -0.9353 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5831   -0.3318   -1.7938 C   0  0  2  0  0  0  0  0  0  0  0  0
   -8.6393    0.2219   -3.2429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.0122   -1.7609   -1.8615 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.3409   -2.1319   -2.3915 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2666   -2.6398   -1.4783 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6909   -2.6832   -0.0721 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.4914   -1.0002    0.6097 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9392   -1.9585    0.9901 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.9189   -1.6093   -1.1639 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.9992   -0.0390   -0.8156 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.8349   -2.3841   -2.4060 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.5527   -0.8243   -3.0943 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.0002    0.4781   -1.8114 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2697   -0.9977   -1.0596 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2905   -0.2264   -4.0071 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.5929   -1.7936   -3.3539 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1220   -0.5485   -1.9107 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8256   -0.2015   -3.6491 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3890    1.5643   -1.6222 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3042    1.9337   -3.3563 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5881    3.2266   -2.1615 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8253    1.9924   -3.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3690    1.5847   -0.1641 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5454    0.4673   -1.2887 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8799    2.2868   -1.8012 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7673    3.3642   -0.6882 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8201    2.4558    0.4594 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3571    1.9538    1.2190 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2841   -0.2316    0.1206 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8330    0.2105   -0.8166 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4405   -1.3006    1.1318 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1940   -0.1008    2.2083 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4193    1.4848    1.9413 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7976   -0.1097    2.4551 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0004   -0.6174    0.1907 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6811    0.9530   -0.4329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8555    2.2137    0.9708 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6534    1.0671   -0.1061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9686   -0.5512    1.6814 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0986    0.4256    2.8777 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7496    2.2333    2.6038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6822    1.2826    1.4354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6034    1.2184    3.7108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3904    0.7598    5.6379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0402    1.3993    4.6055 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2926   -0.3461    4.7582 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6365   -1.1914    4.1946 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2459   -1.5047    3.1285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6431   -0.8547    1.1407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3596   -2.1403    2.1261 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1701    0.7887    2.4828 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8471   -0.7654    3.2379 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6599   -0.1331    0.3108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4207   -1.6310    1.0780 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2052    1.3112    1.4318 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.8514   -0.0229    2.4752 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4762    0.7323    0.9043 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0867   -1.0019    0.5415 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2134    1.5463   -1.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.5225    0.4339   -1.4533 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5409   -0.2877   -1.5375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8749    1.0188   -3.3335 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6560    0.6217   -3.3756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4645   -0.6312   -3.9147 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2744   -3.0011   -3.0976 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.8280   -1.3085   -2.9407 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9992   -2.4022   -1.5183 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 30 31  1  0
 30 32  2  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  2 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  5 42  1  0
  5 43  1  0
  6 44  1  0
  6 45  1  0
  7 46  1  0
  7 47  1  0
  8 48  1  0
  8 49  1  0
  9 50  1  0
  9 51  1  0
 10 52  1  0
 10 53  1  0
 11 54  1  0
 11 55  1  0
 12 56  1  0
 12 57  1  0
 13 58  1  0
 13 59  1  0
 14 60  1  0
 14 61  1  0
 15 62  1  0
 15 63  1  0
 16 64  1  0
 16 65  1  0
 17 66  1  0
 17 67  1  0
 18 68  1  0
 18 69  1  0
 19 70  1  1
 20 71  1  0
 20 72  1  0
 20 73  1  0
 21 74  1  0
 21 75  1  0
 22 76  1  0
 22 77  1  0
 23 78  1  0
 23 79  1  0
 24 80  1  0
 24 81  1  0
 25 82  1  0
 25 83  1  0
 26 84  1  0
 26 85  1  0
 27 86  1  0
 27 87  1  0
 28 88  1  1
 29 89  1  0
 29 90  1  0
 29 91  1  0
 31 92  1  0
 31 93  1  0
 31 94  1  0
M  END


  Mrv1533004151516362D          

 32 31  0  0  0  0            999 V2000
   15.3730    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.0875    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.8020    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.5164    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.2309    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   18.9454    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.6599    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.3743    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.0888    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   21.8033    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.5177    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.2322    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   23.9467    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   24.6612    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   25.3756    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.0901    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   26.8046    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   27.5190    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.2335    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.2335   10.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   28.9480    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   29.6624    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   30.3769    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.0914    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   31.8059    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   32.5203    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.2348    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.9493    9.7006    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   33.9493   10.5256    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   34.6637    9.2881    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   35.3782    9.7006    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   34.6637    8.4631    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 28 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0293988

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCCCCCCCCCCCC(C)CCCCCCCC(C)C(C)=O

> <INCHI_IDENTIFIER>
InChI=1S/C31H62O/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-23-26-29(2)27-24-21-19-22-25-28-30(3)31(4)32/h29-30H,5-28H2,1-4H3

> <INCHI_KEY>
GQJLFAGGBJJGDA-UHFFFAOYSA-N

> <FORMULA>
C31H62O

> <MOLECULAR_WEIGHT>
450.836

> <EXACT_MASS>
450.480066616

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
64.45170598246058

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
3,11-dimethylnonacosan-2-one

> <ALOGPS_LOGP>
10.67

> <JCHEM_LOGP>
12.751037655

> <ALOGPS_LOGS>
-7.67

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
0

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
19.51374428727294

> <JCHEM_PKA_STRONGEST_BASIC>
-7.3407926980304445

> <JCHEM_POLAR_SURFACE_AREA>
17.07

> <JCHEM_REFRACTIVITY>
144.9698

> <JCHEM_ROTATABLE_BOND_COUNT>
26

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.56e-06 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3,11-dimethylnonacosan-2-one

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 15-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   15-APR-15         0                                  
HETATM    1  C   UNK     0      28.696  18.108   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      30.030  17.338   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      31.364  18.108   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      32.697  17.338   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      34.031  18.108   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      35.365  17.338   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      36.698  18.108   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      38.032  17.338   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      39.366  18.108   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      40.699  17.338   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      42.033  18.108   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      43.367  17.338   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      44.700  18.108   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      46.034  17.338   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      47.368  18.108   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      48.702  17.338   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      50.035  18.108   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      51.369  17.338   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      52.703  18.108   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      52.703  19.648   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      54.036  17.338   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      55.370  18.108   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      56.704  17.338   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      58.037  18.108   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      59.371  17.338   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      60.705  18.108   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      62.038  17.338   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      63.372  18.108   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      63.372  19.648   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      64.706  17.338   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0      66.039  18.108   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      64.706  15.798   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27   29   30                                                  
CONECT   29   28                                                            
CONECT   30   28   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   62    0
END

View in JSmol

Synonyms

Value	Source
3,11-Dimethylnonacosanone	MeSH
3,11,-Dimethylnonacosan-2-one	MeSH

Chemical Formula

C₃₁H₆₂O

Average Mass

450.8360 Da

Monoisotopic Mass

450.48007 Da

IUPAC Name

3,11-dimethylnonacosan-2-one

Traditional Name

3,11-dimethylnonacosan-2-one

CAS Registry Number

Not Available

SMILES

CCCCCCCCCCCCCCCCCCC(C)CCCCCCCC(C)C(C)=O

InChI Identifier

InChI=1S/C31H62O/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-23-26-29(2)27-24-21-19-22-25-28-30(3)31(4)32/h29-30H,5-28H2,1-4H3

InChI Key

GQJLFAGGBJJGDA-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Blattella germanica	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as ketones. These are organic compounds in which a carbonyl group is bonded to two carbon atoms R2C=O (neither R may be a hydrogen atom). Ketones that have one or more alpha-hydrogen atoms undergo keto-enol tautomerization, the tautomer being an enol.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbonyl compounds

Direct Parent

Ketones

Alternative Parents

Substituents

Ketone
Organic oxide
Hydrocarbon derivative
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Oxygenated hydrocarbons (LMFA12000235 )

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	10.67	ALOGPS
logP	12.75	ChemAxon
logS	-7.7	ALOGPS
pKa (Strongest Acidic)	19.51	ChemAxon
pKa (Strongest Basic)	-7.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	17.07 Å²	ChemAxon
Rotatable Bond Count	26	ChemAxon
Refractivity	144.97 m³·mol⁻¹	ChemAxon
Polarizability	64.45 Å³	ChemAxon
Number of Rings	0	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

205987

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 3,11-dimethylnonacosan-2-one (NP0293988)

MOL for NP0293988 (3,11-dimethylnonacosan-2-one)

3D MOL for NP0293988 (3,11-dimethylnonacosan-2-one)

3D SDF for NP0293988 (3,11-dimethylnonacosan-2-one)

3D-SDF for NP0293988 (3,11-dimethylnonacosan-2-one)

PDB for NP0293988 (3,11-dimethylnonacosan-2-one)

3D PDB for NP0293988 (3,11-dimethylnonacosan-2-one)

SMILES for NP0293988 (3,11-dimethylnonacosan-2-one)

INCHI for NP0293988 (3,11-dimethylnonacosan-2-one)

Structure for NP0293988 (3,11-dimethylnonacosan-2-one)

3D Structure for NP0293988 (3,11-dimethylnonacosan-2-one)