NP-MRD: Showing NP-Card for (1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol (NP0187743)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-04 03:57:56 UTC

Updated at

2022-09-04 03:57:56 UTC

NP-MRD ID

NP0187743

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol

Description

(1S,2S,4aR,5R,8R,8aR)-8-[(2S,5S)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-decahydronaphthalen-2-ol belongs to the class of organic compounds known as biflorane and serrulatane diterpenoids. These are diterpenoids with a structure based either on the biflorane or the serrulatane skeleton. Based on a literature review very few articles have been published on (1S,2S,4aR,5R,8R,8aR)-8-[(2S,5S)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-decahydronaphthalen-2-ol.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309042205572D          

 27 29  0  0  1  0            999 V2000
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0454    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    1.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9185    2.0890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4488    2.7210    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.1060    2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882    3.0075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3915    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5757    1.6002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3882   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276   -2.2820    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6098   -3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1100   -0.3837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2773    0.2871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
  6 15  1  1  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  1  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  6  0  0  0
M  END

     RDKit          3D

 64 66  0  0  0  0  0  0  0  0999 V2000
   -1.0719   -3.0952   -2.2762 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2177   -1.8883   -1.8951 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4597   -1.6773   -0.4844 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0066   -0.2865   -0.0550 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3782    0.0443   -0.4147 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5090   -0.5222    0.3752 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.6386   -2.0483    0.2313 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4151   -0.1374    1.8178 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6937   -0.5601    2.5624 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7664    0.3113    1.9444 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5125    2.0324    2.2736 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.8009    0.0948    0.4607 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5162    1.3437   -0.1076 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8373   -1.0151    0.2256 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6668   -0.0398   -0.2076 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5364    1.5593   -0.3270 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5372    2.2271    0.4673 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8129    2.1048   -0.3275 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9411    2.5925    0.5107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6753    3.0314   -1.4433 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5788    4.2988   -1.1818 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8974    0.7070   -0.8226 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.3246    0.3157   -0.8427 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6995   -0.7283    0.1611 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8960   -1.9578   -0.2413 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.6164   -2.5263   -1.4710 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1302   -2.9023    0.7785 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1197   -3.9427   -1.6123 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8902   -3.2839   -3.3222 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9129   -2.4376    0.1373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2234   -0.1983    1.0144 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5474   -0.2573   -1.4877 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2491   -2.5831    1.0962 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7308   -2.3512    0.2154 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2888   -2.3964   -0.7600 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5169   -0.4749    2.3124 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4425    0.9699    1.8722 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5721   -0.2798    3.6193 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9444   -1.6038    2.3930 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7258   -0.0025    2.4058 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7827    2.0267   -0.5816 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2068    1.0540   -0.9451 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1257    1.8377    0.6526 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8550   -1.7298    1.0974 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7444   -1.4888   -0.7477 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8802   -0.5827    0.2594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4702    1.9890   -1.3688 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4914    1.8882    0.0693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7391    1.8326    1.4564 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2950    3.2861    0.5489 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5323    3.4370    1.1443 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3611    1.8791    1.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7423    3.1039   -0.1013 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5974    4.6847   -0.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4758    5.0083   -1.9901 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4604    0.6979   -1.8659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0265    1.1977   -0.7654 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5615   -0.1123   -1.8562 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4438   -0.5122    1.1932 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7660   -0.9897    0.0030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2968   -2.0556   -2.4030 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7152   -2.3481   -1.3884 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4956   -3.6219   -1.5423 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3253   -2.9180    1.3508 H   0  0  0  0  0  0  0  0  0  0  0  0
 13 12  1  0
 12 14  1  0
 12 15  1  0
 15  6  1  0
  6  7  1  1
  6  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
  6  5  1  0
  5 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 18 20  1  6
 20 21  2  3
 18 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 25 27  1  1
 25  3  1  0
  3  2  1  0
  2  1  2  3
  3  4  1  0
 10 12  1  0
  4  5  1  0
  4 22  1  0
 13 41  1  0
 13 42  1  0
 13 43  1  0
 14 44  1  0
 14 45  1  0
 14 46  1  0
  7 33  1  0
  7 34  1  0
  7 35  1  0
  8 36  1  0
  8 37  1  0
  9 38  1  0
  9 39  1  0
 10 40  1  1
  5 32  1  6
 16 47  1  0
 16 48  1  0
 17 49  1  0
 17 50  1  0
 19 51  1  0
 19 52  1  0
 19 53  1  0
 21 54  1  0
 21 55  1  0
 22 56  1  6
 23 57  1  0
 23 58  1  0
 24 59  1  0
 24 60  1  0
 26 61  1  0
 26 62  1  0
 26 63  1  0
 27 64  1  0
  3 30  1  1
  1 28  1  0
  1 29  1  0
  4 31  1  1
M  END


  Mrv1652309042205572D          

 27 29  0  0  1  0            999 V2000
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8579    0.0000    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.8579    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.0454    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6704    0.6817    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2007    1.3137    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9185    2.0890    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4488    2.7210    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    3.1060    2.2322    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3882    3.0075    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3915    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5757    1.6002    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579   -1.6500    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3882   -2.2820    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3276   -2.2820    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.6098   -3.0572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.4289   -1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.1100   -0.3837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2773    0.2871    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  3  2  1  1  0  0  0
  4  3  1  1  0  0  0
  4  5  1  0  0  0  0
  5  6  1  6  0  0  0
  6  7  1  6  0  0  0
  6  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  1  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 12 15  1  0  0  0  0
  6 15  1  1  0  0  0
  5 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  6  0  0  0
 18 20  1  1  0  0  0
 20 21  2  0  0  0  0
 18 22  1  0  0  0  0
  4 22  1  0  0  0  0
 22 23  1  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
  3 25  1  0  0  0  0
 25 26  1  1  0  0  0
 25 27  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0187743

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1(C)O[C@@](C)(CC[C@@H]1Cl)[C@@H]1CC[C@@](C)(N=C)[C@@H]2CC[C@](C)(O)[C@@H](N=C)[C@@H]12

> <INCHI_IDENTIFIER>
InChI=1S/C22H37ClN2O2/c1-19(2)16(23)10-13-22(5,27-19)15-8-11-20(3,25-7)14-9-12-21(4,26)18(24-6)17(14)15/h14-18,26H,6-13H2,1-5H3/t14-,15-,16+,17-,18+,20-,21+,22+/m1/s1

> <INCHI_KEY>
QOEVUIRXHICMBB-QAYPUQKFSA-N

> <FORMULA>
C22H37ClN2O2

> <MOLECULAR_WEIGHT>
397.0

> <EXACT_MASS>
396.2543561

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
44.664290874839025

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,2S,4aR,5R,8R,8aR)-8-[(2S,5S)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-decahydronaphthalen-2-ol

> <JCHEM_LOGP>
2.8504307490000005

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
2

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.179374246499833

> <JCHEM_PKA_STRONGEST_BASIC>
7.543123800088999

> <JCHEM_POLAR_SURFACE_AREA>
54.18000000000001

> <JCHEM_REFRACTIVITY>
108.9963

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1S,2S,4aR,5R,8R,8aR)-8-[(2S,5S)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-22         0                                  
HETATM    1  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    2  N   UNK     0       2.667   1.540   0.000  0.00  0.00           N+0
HETATM    3  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       5.335   1.540   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       3.818   1.273   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       6.851   1.273   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       7.841   2.452   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       7.315   3.899   0.000  0.00  0.00           C+0
HETATM   11 Cl   UNK     0       8.304   5.079   0.000  0.00  0.00          Cl+0
HETATM   12  C   UNK     0       5.798   4.167   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       6.325   5.614   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.464   4.937   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.808   2.987   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       6.668  -0.770   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       5.335  -3.080   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.325  -4.260   0.000  0.00  0.00           C+0
HETATM   20  N   UNK     0       4.345  -4.260   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0       4.872  -5.707   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -0.205  -0.716   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       0.518   0.536   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   25                                                  
CONECT    4    3    5   22                                                  
CONECT    5    4    6   16                                                  
CONECT    6    5    7    8   15                                             
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   14   15                                             
CONECT   13   12                                                            
CONECT   14   12                                                            
CONECT   15   12    6                                                       
CONECT   16    5   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   20   22                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20                                                            
CONECT   22   18    4   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24    3   26   27                                             
CONECT   26   25                                                            
CONECT   27   25                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   58    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₂H₃₇ClN₂O₂

Average Mass

397.0000 Da

Monoisotopic Mass

396.25436 Da

IUPAC Name

(1S,2S,4aR,5R,8R,8aR)-8-[(2S,5S)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-decahydronaphthalen-2-ol

Traditional Name

(1S,2S,4aR,5R,8R,8aR)-8-[(2S,5S)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol

CAS Registry Number

Not Available

SMILES

CC1(C)O[C@@](C)(CC[C@@H]1Cl)[C@@H]1CC[C@@](C)(N=C)[C@@H]2CC[C@](C)(O)[C@@H](N=C)[C@@H]12

InChI Identifier

InChI=1S/C22H37ClN2O2/c1-19(2)16(23)10-13-22(5,27-19)15-8-11-20(3,25-7)14-9-12-21(4,26)18(24-6)17(14)15/h14-18,26H,6-13H2,1-5H3/t14-,15-,16+,17-,18+,20-,21+,22+/m1/s1

InChI Key

QOEVUIRXHICMBB-QAYPUQKFSA-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biflorane and serrulatane diterpenoids. These are diterpenoids with a structure based either on the biflorane or the serrulatane skeleton.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Diterpenoids

Direct Parent

Biflorane and serrulatane diterpenoids

Alternative Parents

Substituents

Biflorane diterpenoid
Oxane
Cyclic alcohol
Tertiary alcohol
Dialkyl ether
Ether
Propargyl-type 1,3-dipolar organic compound
Organic 1,3-dipolar compound
Organoheterocyclic compound
Oxacycle
Organic oxygen compound
Organooxygen compound
Organonitrogen compound
Organochloride
Organohalogen compound
Imine
Organopnictogen compound
Hydrocarbon derivative
Alkyl chloride
Alkyl halide
Organic nitrogen compound
Alcohol
Aliphatic heteropolycyclic compound

Molecular Framework

Aliphatic heteropolycyclic compounds

External Descriptors

Not Available

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	2.85	ChemAxon
pKa (Strongest Acidic)	14.18	ChemAxon
pKa (Strongest Basic)	7.54	ChemAxon
Physiological Charge	2	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	54.18 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	109 m³·mol⁻¹	ChemAxon
Polarizability	44.66 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

163084288

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol (NP0187743)

MOL for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

3D MOL for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

3D SDF for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

3D-SDF for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

PDB for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

3D PDB for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

SMILES for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

INCHI for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

Structure for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)

3D Structure for NP0187743 ((1s,2s,4ar,5r,8r,8ar)-8-[(2s,5s)-5-chloro-2,6,6-trimethyloxan-2-yl]-2,5-dimethyl-1,5-bis(methylideneamino)-octahydronaphthalen-2-ol)