NP-MRD: Showing NP-Card for methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate (NP0287540)

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Record Information

Version

2.0

Created at

2022-09-09 16:43:46 UTC

Updated at

2022-09-09 16:43:47 UTC

NP-MRD ID

NP0287540

Secondary Accession Numbers

None

Natural Product Identification

Common Name

methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate

Description

Methyl 2-(3-hydroxy-5-oxo-4-phenyl-2,5-dihydrofuran-2-ylidene)-2-(2-methoxyphenyl)acetate belongs to the class of organic compounds known as anisoles. These are organic compounds containing a methoxybenzene or a derivative thereof. methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate is found in Chrysothrix candelaris. Methyl 2-(3-hydroxy-5-oxo-4-phenyl-2,5-dihydrofuran-2-ylidene)-2-(2-methoxyphenyl)acetate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161501432D          

 26 28  0  0  0  0            999 V2000
   -0.1067   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4748   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9899   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1694   -4.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3188   -3.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -1.7116    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
  5  3  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END

     RDKit          3D

 42 44  0  0  0  0  0  0  0  0999 V2000
   -3.9165   -3.9431   -0.3747 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1904   -2.7865   -0.0360 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8504   -2.6217   -0.2869 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2143   -3.5343   -0.8460 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1812   -1.3979    0.0947 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1032   -1.2748   -0.1614 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8880   -2.2468   -0.7923 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1890   -1.7859   -0.8928 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1035   -2.4725   -1.4249 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2336   -0.4617   -0.2990 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4076    0.3822   -0.2019 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6289   -0.2066    0.1688 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7837    0.5278    0.2663 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7402    1.8756   -0.0067 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5621    2.4872   -0.3730 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4187    1.7168   -0.4613 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0202   -0.1630    0.1283 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5915    0.9942    0.7666 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9742   -0.3337    0.6670 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5514   -0.5768    1.8969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3491    0.3963    2.4482 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5613    1.5766    1.7874 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9844    1.8156    0.5601 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1818    0.8638   -0.0208 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6036    1.0948   -1.2577 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8441    2.3207   -1.9106 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6479   -4.1160    0.4610 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4572   -3.8613   -1.3303 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2800   -4.8478   -0.4275 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6271   -1.2886    0.3807 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.7138    0.0199    0.5593 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6391    2.4663    0.0667 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.5174    3.5610   -0.5928 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5180    2.2324   -0.7593 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4807    1.8774    0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3755   -1.5235    2.4163 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8088    0.1954    3.4330 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2056    2.3285    2.2652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1994    2.7837    0.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9313    2.5643   -1.9247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3048    3.1193   -1.3866 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5532    2.2426   -2.9969 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
  3  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 17  2  0
 17 18  1  0
 10 11  1  0
 11 12  2  0
 12 13  1  0
 13 14  2  0
 14 15  1  0
 15 16  2  0
  5 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  2  0
 24 25  1  0
 25 26  1  0
 17  6  1  0
 16 11  1  0
 24 19  1  0
  1 27  1  0
  1 28  1  0
  1 29  1  0
 18 35  1  0
 12 30  1  0
 13 31  1  0
 14 32  1  0
 15 33  1  0
 16 34  1  0
 20 36  1  0
 21 37  1  0
 22 38  1  0
 23 39  1  0
 26 40  1  0
 26 41  1  0
 26 42  1  0
M  END


  Mrv1533004161501432D          

 26 28  0  0  0  0            999 V2000
   -0.1067   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6078   -0.4741    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3222    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0367   -1.2991    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7041   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4492   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9341   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6242   -2.5687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3693   -1.7840    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5846   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1393   -3.2361    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4748   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9899   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1694   -4.5710    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1661   -3.8173    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3188   -3.1499    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7512    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656    1.1759    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801    0.7634    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -0.0616    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4656   -1.2991    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1801   -1.7116    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
  5  3  1  4  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
  6 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 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
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 13 18  1  0  0  0  0
  5 19  1  0  0  0  0
 19 20  2  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 23 24  2  0  0  0  0
 19 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0287540

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC(=O)C(=C1OC(=O)C(=C1O)C1=CC=CC=C1)C1=CC=CC=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C20H16O6/c1-24-14-11-7-6-10-13(14)16(19(22)25-2)18-17(21)15(20(23)26-18)12-8-4-3-5-9-12/h3-11,21H,1-2H3

> <INCHI_KEY>
IWYVMUDIEOXASM-UHFFFAOYSA-N

> <FORMULA>
C20H16O6

> <MOLECULAR_WEIGHT>
352.342

> <EXACT_MASS>
352.094688235

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
35.809260320578694

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
methyl 2-(3-hydroxy-5-oxo-4-phenyl-2,5-dihydrofuran-2-ylidene)-2-(2-methoxyphenyl)acetate

> <ALOGPS_LOGP>
2.97

> <JCHEM_LOGP>
3.0698446020000003

> <ALOGPS_LOGS>
-4.33

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
5.934212078069298

> <JCHEM_PKA_STRONGEST_BASIC>
-4.854382072823377

> <JCHEM_POLAR_SURFACE_AREA>
82.06

> <JCHEM_REFRACTIVITY>
95.35450000000003

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.63e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0      -0.199  -0.115   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0       1.134  -0.885   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0       2.468  -0.115   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0       2.468   1.425   0.000  0.00  0.00           O+0
HETATM    5  C   UNK     0       3.802  -0.885   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       3.802  -2.425   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0       5.048  -3.330   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       4.572  -4.795   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       5.477  -6.041   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       3.032  -4.795   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.556  -3.330   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       1.091  -2.854   0.000  0.00  0.00           O+0
HETATM   13  C   UNK     0       2.127  -6.041   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.753  -7.448   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       1.848  -8.693   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       0.316  -8.532   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -0.310  -7.126   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.595  -5.880   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       5.136  -0.115   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       5.136   1.425   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       6.469   2.195   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       7.803   1.425   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       7.803  -0.115   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.469  -0.885   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       6.469  -2.425   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0       7.803  -3.195   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   19                                                  
CONECT    6    5    7   11                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   13                                                  
CONECT   11   10    6   12                                                  
CONECT   12   11                                                            
CONECT   13   10   14   18                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   13                                                       
CONECT   19    5   20   24                                                  
CONECT   20   19   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   19   25                                                  
CONECT   25   24   26                                                       
CONECT   26   25                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   56    0
END

View in JSmol

Synonyms

Value	Source
Methyl 2-(3-hydroxy-5-oxo-4-phenyl-2,5-dihydrofuran-2-ylidene)-2-(2-methoxyphenyl)acetic acid	Generator

Chemical Formula

C₂₀H₁₆O₆

Average Mass

352.3420 Da

Monoisotopic Mass

352.09469 Da

IUPAC Name

methyl 2-(3-hydroxy-5-oxo-4-phenyl-2,5-dihydrofuran-2-ylidene)-2-(2-methoxyphenyl)acetate

Traditional Name

methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate

CAS Registry Number

Not Available

SMILES

COC(=O)C(=C1OC(=O)C(=C1O)C1=CC=CC=C1)C1=CC=CC=C1OC

InChI Identifier

InChI=1S/C20H16O6/c1-24-14-11-7-6-10-13(14)16(19(22)25-2)18-17(21)15(20(23)26-18)12-8-4-3-5-9-12/h3-11,21H,1-2H3

InChI Key

IWYVMUDIEOXASM-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

Species Name	Source	Reference
Chrysothrix candelaris	LOTUS Database	35616633

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
Anisole
Methoxybenzene
Alkyl aryl ether
Monocyclic benzene moiety
2-furanone
Dicarboxylic acid or derivatives
Vinylogous acid
Alpha,beta-unsaturated carboxylic ester
Enoate ester
Methyl ester
Dihydrofuran
Enol ester
Carboxylic acid ester
Lactone
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Ether
Enol
Carbonyl group
Organic oxide
Organooxygen compound
Hydrocarbon derivative
Organic oxygen compound
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	2.97	ALOGPS
logP	3.07	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Acidic)	5.93	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	82.06 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	95.35 m³·mol⁻¹	ChemAxon
Polarizability	35.81 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

76179594

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate (NP0287540)

MOL for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

3D MOL for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

3D SDF for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

3D-SDF for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

PDB for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

3D PDB for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

SMILES for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

INCHI for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

Structure for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)

3D Structure for NP0287540 (methyl 2-(3-hydroxy-5-oxo-4-phenylfuran-2-ylidene)-2-(2-methoxyphenyl)acetate)