NP-MRD: Showing NP-Card for methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate (NP0261402)

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Record Information

Version

2.0

Created at

2022-09-08 03:50:21 UTC

Updated at

2022-09-08 03:50:21 UTC

NP-MRD ID

NP0261402

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate

Description

Methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenyl-2,5-dihydrofuran-2-carboxylate belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. Based on a literature review very few articles have been published on methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenyl-2,5-dihydrofuran-2-carboxylate.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309082205502D          

 31 33  0  0  0  0            999 V2000
    2.6255   -0.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735   -0.7959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665   -0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.1602    0.0000 O   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
    0.1624   -0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4174    0.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2243    0.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4793    1.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273    1.7295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1822    2.5141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6302    3.1272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1203    1.5579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4317    2.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1768    2.9556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7288    3.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739    4.3534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5358    3.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1347    0.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1830   -3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3507   -2.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3068   -0.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6937   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9091   -0.6605    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
  3  4  2  0  0  0  0
  3  5  1  0  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  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 13 19  2  0  0  0  0
  7 19  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
M  END

     RDKit          3D

 57 59  0  0  0  0  0  0  0  0999 V2000
   -1.8028    2.8825   -0.0568 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0448    1.5090   -0.0452 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9084    0.6621   -1.1253 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5421    1.1274   -2.2177 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2180   -0.7829   -0.9022 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.2546   -1.3136    0.1409 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1524   -1.2112   -0.3315 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7606   -2.2031   -1.0754 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0684   -2.0849   -1.4963 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8154   -0.9514   -1.1786 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1243   -0.8898   -1.6300 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7202   -1.9120   -2.3865 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2120    0.0336   -0.4398 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    1.2472   -0.0777 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9340    1.0648    1.0124 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2280    1.3372    0.9537 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8822    1.8740   -0.2427 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0682    1.0848    2.1736 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8767   -0.0990   -0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0753   -1.5117   -2.0863 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2663   -2.0662   -2.4391 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5111   -2.8034   -3.4687 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2210   -1.6661   -1.4248 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5733   -2.0313   -1.4205 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6004   -0.8969   -0.5023 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4066   -0.3319    0.5963 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0730   -0.3832    1.9140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8686    0.1933    2.9134 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0289    0.8342    2.5580 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3917    0.9023    1.2453 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6020    0.3337    0.2813 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2912    3.2308   -0.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7794    3.4055    0.1179 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2111    3.1011    0.8802 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3527   -0.7185    1.0469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4801   -2.3684    0.3314 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1419   -3.0747   -1.3025 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5022   -2.9034   -2.0851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4096   -1.8876   -3.4538 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8356   -1.7606   -2.3604 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5359   -2.8967   -1.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4387    1.6242   -1.0144 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2288    2.0362    0.1959 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5085    0.6621    1.9525 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9917    1.9305   -0.0665 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5914    2.9237   -0.4690 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7528    1.2049   -1.0989 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4314    0.7734    3.0285 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8033    0.3053    1.8900 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6436    2.0079    2.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4769    0.7254    0.5693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9648   -2.6125   -0.7039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2030   -0.8753    2.2768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5761    0.1381    3.9595 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6683    1.2920    3.3112 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3201    1.4145    0.9501 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8675    0.3746   -0.7585 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  2  0
  5  3  1  6
  5  6  1  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 11 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  3
 16 17  1  0
 16 18  1  0
 13 19  2  0
  5 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  0
 23 25  2  0
 25 26  1  0
 26 27  2  0
 27 28  1  0
 28 29  2  0
 29 30  1  0
 30 31  2  0
 25  5  1  0
 31 26  1  0
 19  7  1  0
  1 32  1  0
  1 33  1  0
  1 34  1  0
  6 35  1  0
  6 36  1  0
  8 37  1  0
  9 38  1  0
 12 39  1  0
 12 40  1  0
 12 41  1  0
 14 42  1  0
 14 43  1  0
 15 44  1  0
 17 45  1  0
 17 46  1  0
 17 47  1  0
 18 48  1  0
 18 49  1  0
 18 50  1  0
 19 51  1  0
 24 52  1  0
 27 53  1  0
 28 54  1  0
 29 55  1  0
 30 56  1  0
 31 57  1  0
M  END


  Mrv1652309082205502D          

 31 33  0  0  0  0            999 V2000
    2.6255   -0.1828    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0735   -0.7959    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2665   -0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5214    0.1602    0.0000 O   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
    0.1624   -0.6244    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4174    0.1602    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2243    0.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4793    1.1164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9273    1.7295    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1822    2.5141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6302    3.1272    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1203    1.5579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4317    2.1710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1768    2.9556    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7288    3.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4739    4.3534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5358    3.3972    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1347    0.7733    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3819   -1.7224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1270   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6119   -3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3020   -2.5070    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1830   -3.1745    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0470   -1.7224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7376   -1.4675    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3507   -2.0195    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1353   -1.7646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3068   -0.9576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6937   -0.4056    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9091   -0.6605    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
  3  4  2  0  0  0  0
  3  5  1  0  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  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 13 19  2  0  0  0  0
  7 19  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  2  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  2  0  0  0  0
 27 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  2  0  0  0  0
 26 31  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0261402

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C1(CC2=CC=C(OC)C(CC=C(C)C)=C2)OC(=O)C(O)=C1C1=CC=CC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H26O6/c1-16(2)10-12-19-14-17(11-13-20(19)29-3)15-25(24(28)30-4)21(22(26)23(27)31-25)18-8-6-5-7-9-18/h5-11,13-14,26H,12,15H2,1-4H3

> <INCHI_KEY>
VAUVWTVBYIPBIM-UHFFFAOYSA-N

> <FORMULA>
C25H26O6

> <MOLECULAR_WEIGHT>
422.477

> <EXACT_MASS>
422.172938557

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
57

> <JCHEM_AVERAGE_POLARIZABILITY>
43.92870804182711

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenyl-2,5-dihydrofuran-2-carboxylate

> <JCHEM_LOGP>
5.0296781243333335

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.753661616752236

> <JCHEM_PKA_STRONGEST_BASIC>
-3.2805484088325834

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
118.2291

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 08-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   08-SEP-22         0                                  
HETATM    1  C   UNK     0       4.901  -0.341   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       3.870  -1.486   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.364  -1.166   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.840   0.299   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       1.334  -2.310   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       0.303  -1.166   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.779   0.299   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       2.285   0.619   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.761   2.084   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.731   3.228   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       2.207   4.693   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0       1.176   5.837   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       0.225   2.908   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -0.806   4.053   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -0.330   5.517   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.361   6.662   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.885   8.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.867   6.341   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.251   1.444   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       2.580  -3.215   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0       2.104  -4.680   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       3.009  -5.926   0.000  0.00  0.00           O+0
HETATM   23  C   UNK     0       0.564  -4.680   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -0.342  -5.926   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       0.088  -3.215   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      -1.377  -2.739   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      -2.521  -3.770   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      -3.986  -3.294   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -4.306  -1.788   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -3.162  -0.757   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -1.697  -1.233   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4    5                                                  
CONECT    4    3                                                            
CONECT    5    3    6   20   25                                             
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   13                                                  
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14   19                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   13    7                                                       
CONECT   20    5   21                                                       
CONECT   21   20   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24   25                                                  
CONECT   24   23                                                            
CONECT   25   23    5   26                                                  
CONECT   26   25   27   31                                                  
CONECT   27   26   28                                                       
CONECT   28   27   29                                                       
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   26                                                       
MASTER        0    0    0    0    0    0    0    0   31    0   66    0
END

View in JSmol

Synonyms

Value	Source
Methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenyl-2,5-dihydrofuran-2-carboxylic acid	Generator

Chemical Formula

C₂₅H₂₆O₆

Average Mass

422.4770 Da

Monoisotopic Mass

422.17294 Da

IUPAC Name

methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenyl-2,5-dihydrofuran-2-carboxylate

Traditional Name

methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate

CAS Registry Number

Not Available

SMILES

COC(=O)C1(CC2=CC=C(OC)C(CC=C(C)C)=C2)OC(=O)C(O)=C1C1=CC=CC=C1

InChI Identifier

InChI=1S/C25H26O6/c1-16(2)10-12-19-14-17(11-13-20(19)29-3)15-25(24(28)30-4)21(22(26)23(27)31-25)18-8-6-5-7-9-18/h5-11,13-14,26H,12,15H2,1-4H3

InChI Key

VAUVWTVBYIPBIM-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 anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof.

Kingdom

Super Class

Class

Sub Class

Direct Parent

Alternative Parents

Substituents

Phenoxy compound
Methoxybenzene
Anisole
Fatty acid ester
Alkyl aryl ether
Fatty acyl
Dicarboxylic acid or derivatives
2-furanone
Monocyclic benzene moiety
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Lactone
Carboxylic acid ester
Oxacycle
Organoheterocyclic compound
Ether
Enol
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
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	5.03	ChemAxon
pKa (Strongest Acidic)	8.75	ChemAxon
pKa (Strongest Basic)	-3.3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	118.23 m³·mol⁻¹	ChemAxon
Polarizability	43.93 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	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

163063826

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate (NP0261402)

MOL for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

3D MOL for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

3D SDF for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

3D-SDF for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

PDB for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

3D PDB for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

SMILES for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

INCHI for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

Structure for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)

3D Structure for NP0261402 (methyl 4-hydroxy-2-{[4-methoxy-3-(3-methylbut-2-en-1-yl)phenyl]methyl}-5-oxo-3-phenylfuran-2-carboxylate)