NP-MRD: Showing NP-Card for 4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate (NP0255941)

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Record Information

Version

2.0

Created at

2022-09-07 20:36:48 UTC

Updated at

2022-09-07 20:36:48 UTC

NP-MRD ID

NP0255941

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate

Description

4-(Chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms. Based on a literature review very few articles have been published on 4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072222362D          

 28 30  0  0  0  0            999 V2000
   -0.0833    4.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1441    4.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9446    3.9282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4289    3.5343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2015    2.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737    2.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2577    2.9205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5449    1.6346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    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
    0.0000   -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  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  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
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7095    2.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4136    2.5210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4419    1.7115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1369    2.1560    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  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  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  9 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END

     RDKit          3D

 61 63  0  0  0  0  0  0  0  0999 V2000
    7.4527   -1.5678   -0.3787 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2972   -0.8622   -0.9846 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3924   -0.0257   -1.9005 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0355   -1.1537   -0.4997 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8569   -0.5695   -0.9714 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.8404   -1.4986   -1.4347 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0024   -2.5875   -2.0213 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6097   -0.9562   -1.1056 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7369    0.3368   -0.5968 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7234    0.8462    0.3159 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6985    0.9792   -0.0536 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1931    1.9858    1.0974 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5695   -0.1787    0.2062 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2673   -1.4870   -0.4235 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3492   -2.5011   -0.1252 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7423   -2.0825   -0.3838 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0183   -0.7865    0.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9036   -1.0087    1.8766 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3774   -0.2684    0.0740 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9788    0.1462   -0.1204 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3217    1.1672   -0.8226 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4016    2.1688   -1.4123 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9673    1.7997   -1.2652 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.2222    3.1145   -1.1532 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1134    0.2114    0.0853 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7249    1.4338    0.2199 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0423   -0.4962    1.3949 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4160   -2.1404    1.2772 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    7.7882   -0.9704    0.4954 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.3214   -1.6373   -1.0650 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1840   -2.5775   -0.0089 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1191    0.1459   -1.7792 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9593    1.0219   -1.4658 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7124    0.1261    1.2126 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1445    1.7805    0.8008 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1065    2.4658    0.7935 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2179    1.3708    2.0053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3972    2.7523    1.1224 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5450   -0.3805    1.3380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0028   -1.4959   -1.4714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3816   -1.9081    0.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2163   -2.9219    0.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1276   -3.3797   -0.8004 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4154   -2.8602   -0.0098 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8718   -1.8525   -1.4451 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0203   -1.5601    2.1919 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9627   -0.0101    2.3599 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8404   -1.5515    2.1868 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1297   -0.9410    0.5757 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5132    0.7322    0.5139 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6140   -0.2384   -1.0112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3861    1.3731   -1.0428 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6847    3.1625   -1.0108 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6915    2.2329   -2.5050 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6896    1.2682   -2.2150 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8009    3.8412   -0.5227 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7784    3.0205   -0.7106 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0519    3.5674   -2.1605 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8282    1.8529   -0.6675 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0847   -0.5963    1.8173 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5137    0.1486    2.1241 H   0  0  0  0  0  0  0  0  0  0  0  0
 24 23  1  0
 23 22  1  0
 22 21  1  0
 21 20  2  0
 20 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 13 11  1  0
 11 12  1  1
 11 10  1  0
 10  9  1  0
  9  8  1  0
  8  6  1  0
  6  7  2  0
  6  5  1  0
  5  4  1  0
  4  2  1  0
  2  1  1  0
  2  3  2  0
  5 25  1  0
 25 26  1  1
 25 27  1  0
 27 28  1  0
 11 23  1  0
 25  9  1  0
 17 20  1  0
 24 56  1  0
 24 57  1  0
 24 58  1  0
 23 55  1  6
 22 53  1  0
 22 54  1  0
 21 52  1  0
 13 39  1  1
 14 40  1  0
 14 41  1  0
 15 42  1  0
 15 43  1  0
 16 44  1  0
 16 45  1  0
 18 46  1  0
 18 47  1  0
 18 48  1  0
 19 49  1  0
 19 50  1  0
 19 51  1  0
 12 36  1  0
 12 37  1  0
 12 38  1  0
 10 34  1  0
 10 35  1  0
  9 33  1  6
  5 32  1  6
  1 29  1  0
  1 30  1  0
  1 31  1  0
 26 59  1  0
 27 60  1  0
 27 61  1  0
M  END


  Mrv1652309072222362D          

 28 30  0  0  0  0            999 V2000
   -0.0833    4.9208    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1441    4.1278    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9446    3.9282    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4289    3.5343    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2015    2.7413    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5737    2.4591    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2577    2.9205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5449    1.6346    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2481    1.4072    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5303    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5303    0.6320    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.0000    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
    0.0000   -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  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434   -1.2375    0.0000 C   0  0  0  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
    1.8163   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0416   -2.3784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7095    2.0912    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4136    2.5210    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4419    1.7115    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1369    2.1560    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  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  0  0  0  0
 11 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 17 18  1  0  0  0  0
 11 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
  9 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 27 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0255941

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC1CC=C2C(CCCC2(C)C)C1(C)CC1OC(=O)C(OC(C)=O)C1(O)CCl

> <INCHI_IDENTIFIER>
InChI=1S/C22H33ClO5/c1-13-8-9-15-16(7-6-10-20(15,3)4)21(13,5)11-17-22(26,12-23)18(19(25)28-17)27-14(2)24/h9,13,16-18,26H,6-8,10-12H2,1-5H3

> <INCHI_KEY>
VHRXKVWBDALPTK-UHFFFAOYSA-N

> <FORMULA>
C22H33ClO5

> <MOLECULAR_WEIGHT>
412.95

> <EXACT_MASS>
412.2016519

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
44.34078886856328

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate

> <JCHEM_LOGP>
3.8534485106666647

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
18.287272636704998

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.89653721464691

> <JCHEM_PKA_STRONGEST_BASIC>
-4.156251657519438

> <JCHEM_POLAR_SURFACE_AREA>
72.83000000000001

> <JCHEM_REFRACTIVITY>
106.72579999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 07-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   07-SEP-22         0                                  
HETATM    1  C   UNK     0      -0.155   9.186   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.269   7.705   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0       1.763   7.333   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      -0.801   6.597   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -0.376   5.117   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.071   4.590   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       2.348   5.452   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0       1.017   3.051   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -0.463   2.627   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -0.990   1.180   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       0.000  -0.000   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.990   1.180   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.000  -3.080   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       4.001  -0.770   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       4.001  -2.310   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       2.667  -3.080   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       3.390  -4.440   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       1.944  -4.440   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -1.324   3.904   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -2.639   4.706   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -2.692   3.195   0.000  0.00  0.00           C+0
HETATM   28 Cl   UNK     0      -3.989   4.025   0.000  0.00  0.00          Cl+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   25                                                  
CONECT    6    5    7    8                                                  
CONECT    7    6                                                            
CONECT    8    6    9                                                       
CONECT    9    8   10   25                                                  
CONECT   10    9   11                                                       
CONECT   11   10   12   13   18                                             
CONECT   12   11                                                            
CONECT   13   11   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   22                                                  
CONECT   18   17   11   19                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17   23   24                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    9    5   26   27                                             
CONECT   26   25                                                            
CONECT   27   25   28                                                       
CONECT   28   27                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
4-(Chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-yl)methyl]oxolan-3-yl acetic acid	Generator

Chemical Formula

C₂₂H₃₃ClO₅

Average Mass

412.9500 Da

Monoisotopic Mass

412.20165 Da

IUPAC Name

4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-1,2,3,5,6,7,8,8a-octahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate

Traditional Name

4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate

CAS Registry Number

Not Available

SMILES

CC1CC=C2C(CCCC2(C)C)C1(C)CC1OC(=O)C(OC(C)=O)C1(O)CCl

InChI Identifier

InChI=1S/C22H33ClO5/c1-13-8-9-15-16(7-6-10-20(15,3)4)21(13,5)11-17-22(26,12-23)18(19(25)28-17)27-14(2)24/h9,13,16-18,26H,6-8,10-12H2,1-5H3

InChI Key

VHRXKVWBDALPTK-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

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Pentoses

Alternative Parents

Substituents

Pentose monosaccharide
Dicarboxylic acid or derivatives
Gamma butyrolactone
Tertiary alcohol
Tetrahydrofuran
Carboxylic acid ester
Chlorohydrin
Halohydrin
Lactone
Carboxylic acid derivative
Oxacycle
Organoheterocyclic compound
Alkyl halide
Alkyl chloride
Hydrocarbon derivative
Organic oxide
Alcohol
Carbonyl group
Organohalogen compound
Organochloride
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	3.85	ChemAxon
pKa (Strongest Acidic)	11.9	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	72.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	106.73 m³·mol⁻¹	ChemAxon
Polarizability	44.34 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

162815987

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate (NP0255941)

MOL for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

3D MOL for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

3D SDF for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

3D-SDF for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

PDB for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

3D PDB for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

SMILES for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

INCHI for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

Structure for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)

3D Structure for NP0255941 (4-(chloromethyl)-4-hydroxy-2-oxo-5-[(1,2,5,5-tetramethyl-2,3,6,7,8,8a-hexahydronaphthalen-1-yl)methyl]oxolan-3-yl acetate)