NP-MRD: Showing NP-Card for (1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate (NP0281809)

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Record Information

Version

2.0

Created at

2022-09-09 08:23:22 UTC

Updated at

2022-09-09 08:23:23 UTC

NP-MRD ID

NP0281809

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate

Description

(1R)-1-[(2R,3R)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate belongs to the class of organic compounds known as coumarans. Coumarans are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring. (1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate is found in Minuria leptophylla. Based on a literature review very few articles have been published on (1R)-1-[(2R,3R)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309092210232D          

 29 30  0  0  1  0            999 V2000
   -3.9360    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5235    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9360    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610    2.1730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985    2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2136    3.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  1  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
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136    2.2201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4685    1.4354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9165    0.8223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1714    0.0377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1095    0.9939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5575    0.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2495    0.5523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8124   -0.4038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  2  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  2  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END

     RDKit          3D

 59 60  0  0  0  0  0  0  0  0999 V2000
   -1.9109    2.0000    1.2276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1054    2.4620    0.0135 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3243    3.9090   -0.1293 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3125    4.6110    0.9046 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1210    1.6795   -1.2294 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.8672    1.9633   -1.8780 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0884    1.2759   -1.1059 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4147    1.6008   -0.9436 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2109    0.8090   -0.1436 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6581   -0.3010    0.4818 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5256   -1.1539    1.3552 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.7920   -2.3568    1.8359 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7506   -1.3955    0.7353 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9762   -0.9015    1.1593 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9910   -0.1757    2.1837 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.2516   -1.1773    0.4813 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6291   -0.1502   -0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7695    1.2243    0.0257 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7080   -0.1737   -1.7437 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3245   -0.5878    0.2893 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5171    0.1725   -0.5007 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9094    0.2036   -0.9414 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.8793   -0.1895   -0.0191 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8513   -1.1188   -0.3566 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8204   -1.5896   -1.5352 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9197   -1.5859    0.5824 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2487   -1.3197   -0.0964 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4114   -2.0249   -1.4063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4238   -1.6275    0.8060 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9256    2.7057    2.0779 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7273    0.9850    1.5228 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4890    4.3507   -1.0878 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9788    1.8620   -1.8821 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8641    2.4787   -1.4378 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2444    1.0868   -0.0313 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7487   -0.5088    2.2534 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4563   -2.9258    2.5231 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3596   -2.9713    1.0233 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9340   -2.0246    2.4591 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.0472   -1.2221    1.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1662   -2.1780    0.0025 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.6378   -0.4959   -0.9466 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3058    1.9924   -0.6520 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8558    1.4892    0.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2922    1.3571    1.0016 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9496    0.6537   -1.7227 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3040   -0.0218   -2.6839 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2220   -1.1612   -1.8232 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1222   -1.4479    0.7701 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0592   -0.3869   -1.8890 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8814   -1.0560    1.5380 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7897   -2.6852    0.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2537   -0.2078   -0.3116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4785   -2.2849   -1.6211 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0828   -1.3957   -2.2824 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8120   -2.9653   -1.4967 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3436   -2.5584    1.3620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3559   -1.6307    0.1748 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5558   -0.7779    1.5246 H   0  0  0  0  0  0  0  0  0  0  0  0
 18 17  1  0
 17 19  1  0
 17 16  1  0
 16 14  1  0
 14 15  2  0
 14 13  1  0
 13 11  1  0
 11 12  1  0
 11 10  1  0
 10  9  2  0
  9  8  1  0
  8  7  2  0
  7  6  1  0
  6  5  1  0
  5 22  1  0
 22 23  1  0
 23 24  1  0
 24 25  2  0
 24 26  1  0
 26 27  1  0
 27 28  1  0
 27 29  1  0
 22 21  1  0
 21 20  2  0
  5  2  1  0
  2  1  2  3
  2  3  1  0
  3  4  2  0
 20 10  1  0
 21  7  1  0
 18 43  1  0
 18 44  1  0
 18 45  1  0
 17 42  1  0
 19 46  1  0
 19 47  1  0
 19 48  1  0
 16 40  1  0
 16 41  1  0
 11 36  1  1
 12 37  1  0
 12 38  1  0
 12 39  1  0
  9 35  1  0
  8 34  1  0
  5 33  1  6
 22 50  1  6
 26 51  1  0
 26 52  1  0
 27 53  1  0
 28 54  1  0
 28 55  1  0
 28 56  1  0
 29 57  1  0
 29 58  1  0
 29 59  1  0
 20 49  1  0
  1 30  1  0
  1 31  1  0
  3 32  1  0
M  END


  Mrv1652309092210232D          

 29 30  0  0  1  0            999 V2000
   -3.9360    3.6020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5235    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9360    2.1730    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7610    2.1730    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6985    2.8875    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.2136    3.5549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.0625    0.0000 C   0  0  1  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
    1.4289    2.4750    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8579    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5724    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    2.4750    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
   -0.7145    2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2136    2.2201    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4685    1.4354    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9165    0.8223    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1714    0.0377    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1095    0.9939    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5575    0.3808    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2495    0.5523    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8124   -0.4038    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  2  0  0  0  0
  5  2  1  1  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  6  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 10 20  1  0  0  0  0
 20 21  2  0  0  0  0
  7 21  1  0  0  0  0
 21 22  1  0  0  0  0
  5 22  1  0  0  0  0
 22 23  1  1  0  0  0
 23 24  1  0  0  0  0
 24 25  2  0  0  0  0
 24 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 27 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0281809

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)O[C@H](C)C1=CC=C2O[C@@H]([C@H](OC(=O)CC(C)C)C2=C1)C(=C)C=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H30O6/c1-13(2)9-20(25)27-16(6)17-7-8-19-18(11-17)23(22(28-19)15(5)12-24)29-21(26)10-14(3)4/h7-8,11-14,16,22-23H,5,9-10H2,1-4,6H3/t16-,22-,23-/m1/s1

> <INCHI_KEY>
HVERHDCDLKVVMD-ZGNKEGEESA-N

> <FORMULA>
C23H30O6

> <MOLECULAR_WEIGHT>
402.487

> <EXACT_MASS>
402.204238686

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
43.919704486479475

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(1R)-1-[(2R,3R)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate

> <JCHEM_LOGP>
4.399644716000001

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.861930911800607

> <JCHEM_POLAR_SURFACE_AREA>
78.9

> <JCHEM_REFRACTIVITY>
108.03569999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
1

> <JCHEM_TRADITIONAL_IUPAC>
(1R)-1-[(2R,3R)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 09-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   09-SEP-22         0                                  
HETATM    1  C   UNK     0      -7.347   6.724   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -6.577   5.390   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -7.347   4.056   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0      -8.887   4.056   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0      -5.037   5.390   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0      -4.132   6.636   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0      -2.667   6.160   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.334   6.930   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.000   6.160   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.334   3.850   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0       4.001   3.850   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.668   3.850   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       6.668   2.310   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -1.334   3.850   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -4.132   4.144   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      -4.608   2.679   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      -3.577   1.535   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0      -4.053   0.070   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      -2.071   1.855   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -1.041   0.711   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.466   1.031   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -1.516  -0.754   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    5                                                  
CONECT    3    2    4                                                       
CONECT    4    3                                                            
CONECT    5    2    6   22                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   21                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   20                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11                                                            
CONECT   13   11   14                                                       
CONECT   14   13   15   16                                                  
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18   19                                                  
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   10   21                                                       
CONECT   21   20    7   22                                                  
CONECT   22   21    5   23                                                  
CONECT   23   22   24                                                       
CONECT   24   23   25   26                                                  
CONECT   25   24                                                            
CONECT   26   24   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
MASTER        0    0    0    0    0    0    0    0   29    0   60    0
END

View in JSmol

Synonyms

Value	Source
(1R)-1-[(2R,3R)-3-[(3-Methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoic acid	Generator

Chemical Formula

C₂₃H₃₀O₆

Average Mass

402.4870 Da

Monoisotopic Mass

402.20424 Da

IUPAC Name

(1R)-1-[(2R,3R)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate

Traditional Name

(1R)-1-[(2R,3R)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)O[C@H](C)C1=CC=C2O[C@@H]([C@H](OC(=O)CC(C)C)C2=C1)C(=C)C=O

InChI Identifier

InChI=1S/C23H30O6/c1-13(2)9-20(25)27-16(6)17-7-8-19-18(11-17)23(22(28-19)15(5)12-24)29-21(26)10-14(3)4/h7-8,11-14,16,22-23H,5,9-10H2,1-4,6H3/t16-,22-,23-/m1/s1

InChI Key

HVERHDCDLKVVMD-ZGNKEGEESA-N

Experimental Spectra

Not Available

Predicted Spectra

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

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Minuria leptophylla	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as coumarans. Coumarans are compounds containing the coumaran skeleton, which consists of a benzene ring fused to a 2,3-dihydrofuran ring.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Coumarans

Sub Class

Not Available

Direct Parent

Coumarans

Alternative Parents

Substituents

Coumaran
Alkyl aryl ether
Fatty acid ester
Dicarboxylic acid or derivatives
Fatty acyl
Benzenoid
Alpha,beta-unsaturated aldehyde
Enal
Carboxylic acid ester
Carboxylic acid derivative
Oxacycle
Ether
Hydrocarbon derivative
Aldehyde
Carbonyl group
Organic oxygen compound
Organooxygen compound
Organic oxide
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic 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	4.4	ChemAxon
pKa (Strongest Basic)	-4.9	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	11	ChemAxon
Refractivity	108.04 m³·mol⁻¹	ChemAxon
Polarizability	43.92 Å³	ChemAxon
Number of Rings	2	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

163036352

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate (NP0281809)

MOL for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

3D MOL for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

3D SDF for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

3D-SDF for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

PDB for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

3D PDB for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

SMILES for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

INCHI for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

Structure for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)

3D Structure for NP0281809 ((1r)-1-[(2r,3r)-3-[(3-methylbutanoyl)oxy]-2-(3-oxoprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-5-yl]ethyl 3-methylbutanoate)