NP-MRD: Showing NP-Card for (1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate (NP0242539)

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Record Information

Version

2.0

Created at

2022-09-07 02:52:45 UTC

Updated at

2022-09-07 02:52:45 UTC

NP-MRD ID

NP0242539

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate

Description

[(2R,3R)-3-[(1S)-1-(benzoyloxy)-5-methylhexyl]-4-oxooxolan-2-yl]methyl benzoate belongs to the class of organic compounds known as benzoic acid esters. These are ester derivatives of benzoic acid. Based on a literature review very few articles have been published on [(2R,3R)-3-[(1S)-1-(benzoyloxy)-5-methylhexyl]-4-oxooxolan-2-yl]methyl benzoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309072204522D          

 32 34  0  0  1  0            999 V2000
   -1.9947   -1.3566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7247   -2.1362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2648   -2.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9146   -2.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3745   -1.6685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4357   -1.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9758   -1.2007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7859   -1.3566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0559   -2.1362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.2921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5159   -2.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859   -3.5394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2458   -4.1630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4357   -4.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1656   -3.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7057   -2.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7057   -0.4212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1777    0.2555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0025    0.2714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6799    0.9135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0996    0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0837   -0.1814    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7416   -0.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5016   -0.3582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6037    0.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9458    0.9582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3637    0.7814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0217    0.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7817    0.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8838    1.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2258    1.9210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658    1.6000    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
  2  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  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 17  7  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 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  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END

     RDKit          3D

 62 64  0  0  0  0  0  0  0  0999 V2000
   -5.5907    4.5233    1.5543 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2585    4.0629    1.0517 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9812    4.4817   -0.3650 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2051    2.5376    1.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8429    2.1412    0.5714 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6614    0.6411    0.5568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2712    0.2696    0.0268 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2441   -1.1410    0.0685 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3040   -1.9184   -1.0939 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3832   -1.2804   -2.1732 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2763   -3.3767   -1.0575 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1910   -4.0900    0.0970 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1696   -5.4857    0.0514 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2328   -6.1797   -1.1399 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3192   -5.4506   -2.3074 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3404   -4.0529   -2.2578 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1811    0.9792    0.6832 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0153    0.8247    2.1268 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6162    0.3917    3.0431 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4012    1.4056    2.3250 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9204    1.5915    1.0345 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2282    0.6575    0.2095 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7157   -0.6810    0.6545 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1136   -0.7670    0.4912 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.7356   -0.6545   -0.7322 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9790   -0.4668   -1.7433 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1731   -0.7385   -0.9112 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7118   -0.6153   -2.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0892   -0.6908   -2.3781 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9254   -0.8905   -1.3205 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4151   -1.0176   -0.0491 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0316   -0.9396    0.1448 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5927    4.3990    2.6652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3617    3.8329    1.1626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8239    5.5613    1.2472 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4063    4.4040    1.6905 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8789    4.6352   -0.4963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4745    5.4431   -0.5758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3076    3.7159   -1.1074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0291    2.1058    0.4957 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3354    2.2032    2.1427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0974    2.6667    1.1942 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7531    2.5463   -0.4572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3693    0.2387   -0.1980 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8909    0.1653    1.5076 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3258    0.6370   -1.0442 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1414   -3.5502    1.0296 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1025   -6.0466    0.9590 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2142   -7.2659   -1.1444 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3685   -5.9956   -3.2374 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4090   -3.5238   -3.1990 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2672    2.0983    0.5112 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0199    0.7924    2.9756 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2374    2.4431    2.7279 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4024    0.9331   -0.8213 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.5251   -0.7572    1.7615 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2644   -1.5416    0.1176 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0936   -0.4557   -3.0427 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4680   -0.5884   -3.3837 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.9902   -0.9473   -1.4951 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0727   -1.1737    0.7752 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6893   -1.0458    1.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  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  2  0
  9 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  7 17  1  0
 17 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  2  0
 25 27  1  0
 27 28  2  0
 28 29  1  0
 29 30  2  0
 30 31  1  0
 31 32  2  0
 22 21  1  0
 21 20  1  0
 20 18  1  0
 18 19  2  0
 16 11  1  0
 18 17  1  0
 32 27  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  3 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  6
 12 47  1  0
 13 48  1  0
 14 49  1  0
 15 50  1  0
 16 51  1  0
 17 52  1  1
 22 55  1  6
 23 56  1  0
 23 57  1  0
 28 58  1  0
 29 59  1  0
 30 60  1  0
 31 61  1  0
 32 62  1  0
 20 53  1  0
 20 54  1  0
M  END


  Mrv1652309072204522D          

 32 34  0  0  1  0            999 V2000
   -1.9947   -1.3566    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7247   -2.1362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2648   -2.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9146   -2.2921    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3745   -1.6685    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4357   -1.8244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9758   -1.2007    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.7859   -1.3566    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0559   -2.1362    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8661   -2.2921    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5159   -2.7598    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7859   -3.5394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2458   -4.1630    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4357   -4.0071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1656   -3.2276    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7057   -2.6039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7057   -0.4212    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1777    0.2555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0025    0.2714    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6799    0.9135    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0996    0.6434    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0837   -0.1814    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7416   -0.6792    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5016   -0.3582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6037    0.4604    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9458    0.9582    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3637    0.7814    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0217    0.2837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7817    0.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8838    1.4233    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2258    1.9210    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4658    1.6000    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
  2  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  1  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 13 14  2  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 11 16  1  0  0  0  0
 17  7  1  6  0  0  0
 17 18  1  0  0  0  0
 18 19  2  0  0  0  0
 18 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  6  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  2  0  0  0  0
 25 27  1  0  0  0  0
 27 28  2  0  0  0  0
 28 29  1  0  0  0  0
 29 30  2  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 27 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0242539

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CCC[C@H](OC(=O)C1=CC=CC=C1)[C@@H]1[C@H](COC(=O)C2=CC=CC=C2)OCC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H30O6/c1-18(2)10-9-15-22(32-26(29)20-13-7-4-8-14-20)24-21(27)16-30-23(24)17-31-25(28)19-11-5-3-6-12-19/h3-8,11-14,18,22-24H,9-10,15-17H2,1-2H3/t22-,23-,24+/m0/s1

> <INCHI_KEY>
HRJWHNUFVIACBL-KMDXXIMOSA-N

> <FORMULA>
C26H30O6

> <MOLECULAR_WEIGHT>
438.52

> <EXACT_MASS>
438.204238686

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
62

> <JCHEM_AVERAGE_POLARIZABILITY>
47.962690587338855

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(1S)-1-[(2R,3R)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate

> <JCHEM_LOGP>
6.052802413

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.793709779623644

> <JCHEM_PKA_STRONGEST_BASIC>
-4.216969908423859

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
120.03860000000002

> <JCHEM_ROTATABLE_BOND_COUNT>
12

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(1S)-1-[(2R,3R)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate

> <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      -3.723  -2.532   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.219  -3.988   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -4.228  -5.152   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.707  -4.279   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.699  -3.114   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.813  -3.405   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.821  -2.241   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       3.334  -2.532   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       3.838  -3.988   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       5.350  -4.279   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       2.830  -5.152   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.334  -6.607   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       2.326  -7.771   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       0.813  -7.480   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       0.309  -6.025   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.317  -4.861   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       1.317  -0.786   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.198   0.477   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       3.738   0.507   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.269   1.705   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      -0.186   1.201   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      -0.156  -0.339   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.384  -1.268   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -2.803  -0.669   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -2.994   0.859   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.765   1.789   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0      -4.412   1.459   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -5.640   0.529   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -7.059   1.129   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -7.250   2.657   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -6.022   3.586   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -4.603   2.987   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8   17                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   16                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11                                                       
CONECT   17    7   18   22                                                  
CONECT   18   17   19   20                                                  
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   17   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26   27                                                  
CONECT   26   25                                                            
CONECT   27   25   28   32                                                  
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   27                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

View in JSmol

Synonyms

Value	Source
[(2R,3R)-3-[(1S)-1-(Benzoyloxy)-5-methylhexyl]-4-oxooxolan-2-yl]methyl benzoic acid	Generator

Chemical Formula

C₂₆H₃₀O₆

Average Mass

438.5200 Da

Monoisotopic Mass

438.20424 Da

IUPAC Name

(1S)-1-[(2R,3R)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate

Traditional Name

(1S)-1-[(2R,3R)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate

CAS Registry Number

Not Available

SMILES

CC(C)CCC[C@H](OC(=O)C1=CC=CC=C1)[C@@H]1[C@H](COC(=O)C2=CC=CC=C2)OCC1=O

InChI Identifier

InChI=1S/C26H30O6/c1-18(2)10-9-15-22(32-26(29)20-13-7-4-8-14-20)24-21(27)16-30-23(24)17-31-25(28)19-11-5-3-6-12-19/h3-8,11-14,18,22-24H,9-10,15-17H2,1-2H3/t22-,23-,24+/m0/s1

InChI Key

HRJWHNUFVIACBL-KMDXXIMOSA-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 benzoic acid esters. These are ester derivatives of benzoic acid.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Benzoic acids and derivatives

Direct Parent

Benzoic acid esters

Alternative Parents

Substituents

Benzoate ester
Benzoyl
Dicarboxylic acid or derivatives
3-furanone
Tetrahydrofuran
Carboxylic acid ester
Ketone
Cyclic ketone
Oxacycle
Ether
Dialkyl ether
Carboxylic acid derivative
Organoheterocyclic compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Organooxygen compound
Organic oxide
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic 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	6.05	ChemAxon
pKa (Strongest Acidic)	14.79	ChemAxon
pKa (Strongest Basic)	-4.2	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	78.9 Å²	ChemAxon
Rotatable Bond Count	12	ChemAxon
Refractivity	120.04 m³·mol⁻¹	ChemAxon
Polarizability	47.96 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	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

163188057

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate (NP0242539)

MOL for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

3D MOL for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

3D SDF for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

3D-SDF for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

PDB for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

3D PDB for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

SMILES for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

INCHI for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

Structure for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)

3D Structure for NP0242539 ((1s)-1-[(2r,3r)-2-[(benzoyloxy)methyl]-4-oxooxolan-3-yl]-5-methylhexyl benzoate)