NP-MRD: Showing NP-Card for (1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate (NP0158583)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 16:12:01 UTC

Updated at

2022-09-02 16:12:01 UTC

NP-MRD ID

NP0158583

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate

Description

(1R,3S,3aS,4Z,7aS)-3-(acetyloxy)-4-ethylidene-5-[(1R)-1,3,3-trimethylcyclohexyl]-1,3,3a,4,7,7a-hexahydro-2-benzofuran-1-yl acetate belongs to the class of organic compounds known as isobenzofurans. These are organic aromatic compounds containing an isobenzofuran moiety. Based on a literature review very few articles have been published on (1R,3S,3aS,4Z,7aS)-3-(acetyloxy)-4-ethylidene-5-[(1R)-1,3,3-trimethylcyclohexyl]-1,3,3a,4,7,7a-hexahydro-2-benzofuran-1-yl acetate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022218122D          

 28 30  0  0  1  0            999 V2000
    3.9934    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9900    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1776    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4597    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2722    2.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8025    2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3328    2.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5170    1.7435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5203    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659    1.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630    2.8207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659   -0.5980    0.0000 O   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
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  1  0  0  0
  5  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
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  5 13  1  0  0  0  0
  4 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17  3  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
   -0.6315   -0.1395    2.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5527    0.4245    1.8815 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6942    0.3290    0.5791 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3791   -0.3346   -0.1378 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7476   -0.0309    0.0572 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.8912    0.6694   -1.3698 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4038    1.0594    0.7481 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6163    1.6951    0.0370 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6594    0.6255   -0.0763 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1820   -0.7728   -0.0935 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8913   -1.4701   -1.2805 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8392   -1.4668    1.1229 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7753   -1.1449   -0.1364 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0447   -1.2321   -1.0612 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4995   -1.3876   -1.1851 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2881   -0.1041   -1.2187 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.8951    0.8801   -0.1366 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.1219    0.9702    0.6740 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.3451    2.3311    1.0267 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.6791    2.7725    2.2782 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8934    4.2342    2.5495 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8018    1.9212    3.1960 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1828    0.6674   -0.2253 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7050   -0.4579   -0.8321 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.4688   -0.8809   -1.9400 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0365   -2.1378   -1.9525 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8493   -2.6526   -3.0759 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8401   -2.8700   -0.9441 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1996    0.4854    3.2090 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0772   -0.7454    3.3249 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0892   -1.0397    2.1102 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3484    0.9393    2.4516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9028    0.5776   -1.6808 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3993    1.6338   -1.3554 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3557    0.0502   -2.1507 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0257    0.7192    1.6444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8001    1.9659    0.9917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3748    2.2749   -0.8373 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9646    2.5101    0.7589 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2242    0.8820   -1.0267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4197    0.8284    0.7161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1812   -1.5033   -2.1561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1321   -2.5056   -1.0454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8293   -0.9415   -1.5336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8442   -2.5490    0.8724 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3077   -1.2486    2.0520 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8971   -1.1166    1.1294 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5082   -1.6057   -1.1218 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5763   -2.0205    0.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6175   -1.7839   -1.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8989   -2.0256   -0.3583 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7261   -1.9175   -2.1330 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2704    0.3788   -2.2319 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6263    1.8257   -0.6271 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2351    0.2763    1.4981 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9272    4.7541    1.5886 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8576    4.4110    3.0685 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0509    4.6525    3.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6706   -1.2710   -0.0663 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4531   -3.5233   -2.7398 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2472   -2.9948   -3.9339 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5333   -1.8703   -3.4381 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  1  0
 20 21  1  0
 20 22  2  0
 18 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 26 28  2  0
 24 16  1  0
 16 15  1  0
 15 14  1  0
 14  4  2  0
  4  5  1  0
  5  6  1  6
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 10 13  1  0
  4  3  1  0
 13  5  1  0
 16 17  1  0
  1 29  1  0
  1 30  1  0
  1 31  1  0
  2 32  1  0
 17 54  1  6
 18 55  1  1
 21 56  1  0
 21 57  1  0
 21 58  1  0
 24 59  1  1
 27 60  1  0
 27 61  1  0
 27 62  1  0
 16 53  1  6
 15 51  1  0
 15 52  1  0
 14 50  1  0
  6 33  1  0
  6 34  1  0
  6 35  1  0
  7 36  1  0
  7 37  1  0
  8 38  1  0
  8 39  1  0
  9 40  1  0
  9 41  1  0
 11 42  1  0
 11 43  1  0
 11 44  1  0
 12 45  1  0
 12 46  1  0
 12 47  1  0
 13 48  1  0
 13 49  1  0
M  END


  Mrv1652309022218122D          

 28 30  0  0  1  0            999 V2000
    3.9934    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7079    1.2375    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.9900    0.4623    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1776    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4597    2.6447    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2722    2.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8025    2.1560    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3328    2.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5170    1.7435    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5203    1.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9934    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2789   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5645    0.0000    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5645    0.8250    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7798    1.0799    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5249    1.8646    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179    2.0361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659    1.4230    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630    2.8207    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2949    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7798   -0.2549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5249   -1.0396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7179   -1.2111    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4630   -1.9957    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1659   -0.5980    0.0000 O   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
  3  4  1  0  0  0  0
  5  4  1  6  0  0  0
  5  6  1  1  0  0  0
  5  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
 10 12  1  0  0  0  0
 10 13  1  0  0  0  0
  5 13  1  0  0  0  0
  4 14  2  0  0  0  0
 14 15  1  0  0  0  0
 16 15  1  6  0  0  0
 16 17  1  0  0  0  0
 17  3  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  1  1  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
 18 23  1  0  0  0  0
 23 24  1  0  0  0  0
 16 24  1  0  0  0  0
 24 25  1  1  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  2  0  0  0  0
M  END
> <DATABASE_ID>
NP0158583

> <DATABASE_NAME>
NP-MRD

> <SMILES>
C\C=C1\[C@H]2[C@H](OC(C)=O)O[C@H](OC(C)=O)[C@H]2CC=C1[C@]1(C)CCCC(C)(C)C1

> <INCHI_IDENTIFIER>
InChI=1S/C23H34O5/c1-7-16-18(23(6)12-8-11-22(4,5)13-23)10-9-17-19(16)21(27-15(3)25)28-20(17)26-14(2)24/h7,10,17,19-21H,8-9,11-13H2,1-6H3/b16-7+/t17-,19+,20-,21+,23+/m0/s1

> <INCHI_KEY>
APJJJQRQXHYHMQ-RSXXHTISSA-N

> <FORMULA>
C23H34O5

> <MOLECULAR_WEIGHT>
390.52

> <EXACT_MASS>
390.240624195

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
44.108365794332386

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1S,3R,3aS,7Z,7aS)-3-(acetyloxy)-7-ethylidene-6-[(1R)-1,3,3-trimethylcyclohexyl]-1,3,3a,4,7,7a-hexahydro-2-benzofuran-1-yl acetate

> <ALOGPS_LOGP>
5.63

> <JCHEM_LOGP>
4.306934537999998

> <ALOGPS_LOGS>
-4.96

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.523157899916258

> <JCHEM_POLAR_SURFACE_AREA>
61.830000000000005

> <JCHEM_REFRACTIVITY>
107.41709999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.24e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(1S,3R,3aS,7Z,7aS)-3-(acetyloxy)-7-ethylidene-6-[(1R)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1H-2-benzofuran-1-yl acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0       7.454   4.620   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       6.121   3.850   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       6.121   2.310   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       7.454   1.540   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.788   2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       9.315   0.863   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       7.798   3.490   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.325   4.937   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.841   5.204   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      10.831   4.025   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      11.821   5.204   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.165   3.255   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.305   2.577   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       7.454   0.000   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.121  -0.770   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.787   0.000   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       4.787   1.540   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       3.322   2.016   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       2.846   3.481   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.340   3.801   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.310   2.656   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       0.864   5.265   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       2.417   0.770   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       3.322  -0.476   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       2.846  -1.941   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       1.340  -2.261   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       0.864  -3.725   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0       0.310  -1.116   0.000  0.00  0.00           O+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   17                                                  
CONECT    4    3    5   14                                                  
CONECT    5    4    6    7   13                                             
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   13                                             
CONECT   11   10                                                            
CONECT   12   10                                                            
CONECT   13   10    5                                                       
CONECT   14    4   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   24                                                  
CONECT   17   16    3   18                                                  
CONECT   18   17   19   23                                                  
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   18   24                                                       
CONECT   24   23   16   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27   28                                                  
CONECT   27   26                                                            
CONECT   28   26                                                            
MASTER        0    0    0    0    0    0    0    0   28    0   60    0
END

View in JSmol

Synonyms

Value	Source
(1R,3S,3AS,4Z,7as)-3-(acetyloxy)-4-ethylidene-5-[(1R)-1,3,3-trimethylcyclohexyl]-1,3,3a,4,7,7a-hexahydro-2-benzofuran-1-yl acetic acid	Generator

Chemical Formula

C₂₃H₃₄O₅

Average Mass

390.5200 Da

Monoisotopic Mass

390.24062 Da

IUPAC Name

(1S,3R,3aS,7Z,7aS)-3-(acetyloxy)-7-ethylidene-6-[(1R)-1,3,3-trimethylcyclohexyl]-1,3,3a,4,7,7a-hexahydro-2-benzofuran-1-yl acetate

Traditional Name

(1S,3R,3aS,7Z,7aS)-3-(acetyloxy)-7-ethylidene-6-[(1R)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1H-2-benzofuran-1-yl acetate

CAS Registry Number

Not Available

SMILES

C\C=C1\[C@H]2[C@H](OC(C)=O)O[C@H](OC(C)=O)[C@H]2CC=C1[C@]1(C)CCCC(C)(C)C1

InChI Identifier

InChI=1S/C23H34O5/c1-7-16-18(23(6)12-8-11-22(4,5)13-23)10-9-17-19(16)21(27-15(3)25)28-20(17)26-14(2)24/h7,10,17,19-21H,8-9,11-13H2,1-6H3/b16-7+/t17-,19+,20-,21+,23+/m0/s1

InChI Key

APJJJQRQXHYHMQ-RSXXHTISSA-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 isobenzofurans. These are organic aromatic compounds containing an isobenzofuran moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Isobenzofurans

Sub Class

Not Available

Direct Parent

Isobenzofurans

Alternative Parents

Substituents

Isobenzofuran
Dicarboxylic acid or derivatives
Tetrahydrofuran
Carboxylic acid ester
Oxacycle
Carboxylic acid derivative
Acetal
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	5.63	ALOGPS
logP	4.31	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Basic)	-4.5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	61.83 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	107.42 m³·mol⁻¹	ChemAxon
Polarizability	44.11 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

162977871

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate (NP0158583)

MOL for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

3D MOL for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

3D SDF for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

3D-SDF for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

PDB for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

3D PDB for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

SMILES for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

INCHI for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

Structure for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)

3D Structure for NP0158583 ((1s,3r,3as,7z,7as)-3-(acetyloxy)-7-ethylidene-6-[(1r)-1,3,3-trimethylcyclohexyl]-3,3a,4,7a-tetrahydro-1h-2-benzofuran-1-yl acetate)