NP-MRD: Showing NP-Card for n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid (NP0155037)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-02 12:01:40 UTC

Updated at

2022-09-02 12:01:40 UTC

NP-MRD ID

NP0155037

Secondary Accession Numbers

None

Natural Product Identification

Common Name

n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid

Description

CHEMBL551629 belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups. n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid is found in Wollastonia biflora. Based on a literature review very few articles have been published on CHEMBL551629.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022214012D          

 25 26  0  0  0  0            999 V2000
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 O   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   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 12 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END

     RDKit          3D

 45 46  0  0  0  0  0  0  0  0999 V2000
    7.5818   -1.2712    0.1463 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.0464    0.0315    0.0767 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.6745    0.1814    0.0677 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8406   -0.9000    0.1245 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4711   -0.7437    0.1151 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8652    0.4920    0.0490 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4130    0.6417    0.0399 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6051   -0.3393    0.0914 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7867   -0.2361    0.0848 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4759   -1.2969    0.3224 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8526   -2.5084    0.5779 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9510   -1.1955    0.3172 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7485   -2.2852    0.5623 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1292   -2.2182    0.5635 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6875   -0.9697    0.2992 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0588   -0.8219    0.2827 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8928   -1.9346    0.5333 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9332    0.1477    0.0485 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5261    1.3916   -0.2143 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7892    2.5456   -0.4728 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5541    0.0164    0.0614 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7106    1.5799   -0.0081 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0836    1.4466    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9561    2.5214   -0.0564 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3655    3.8191   -0.1257 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2971   -1.7689   -0.8262 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.6943   -1.2176    0.1565 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1809   -1.8554    0.9876 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2846   -1.8771    0.1767 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8362   -1.6167    0.1610 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9607    1.6357   -0.0133 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2035   -2.8575   -0.1134 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2657   -3.2465    0.7652 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7580   -3.0903    0.7596 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.9602   -1.6216    0.3521 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.8403   -2.2422    1.6066 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6334   -2.7925   -0.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8938    2.6421    0.1956 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4106    3.4423   -0.2804 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4679    2.5145   -1.5454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9267    0.8681   -0.1303 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2757    2.5684   -0.0609 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7584    3.9002   -1.0430 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1437    4.6127   -0.1584 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7008    3.9078    0.7508 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
  4  5  1  0
  5  6  2  0
  6  7  1  0
  7  8  2  0
  8  9  1  0
  9 10  2  0
 10 11  1  0
 10 12  1  0
 12 13  2  0
 13 14  1  0
 14 15  2  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 18 21  2  0
  6 22  1  0
 22 23  2  0
 23 24  1  0
 24 25  1  0
 23  3  1  0
 21 12  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
  4 29  1  0
  5 30  1  0
  7 31  1  0
 11 32  1  0
 13 33  1  0
 14 34  1  0
 17 35  1  0
 17 36  1  0
 17 37  1  0
 20 38  1  0
 20 39  1  0
 20 40  1  0
 21 41  1  0
 22 42  1  0
 25 43  1  0
 25 44  1  0
 25 45  1  0
M  END


  Mrv1652309022214012D          

 25 26  0  0  0  0            999 V2000
   -1.4289   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -2.8875    0.0000 O   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   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -5.3625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145   -6.1875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -6.6000    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -7.4250    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -7.8375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -7.4250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -8.6625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -10.3125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434  -11.1375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289  -11.5500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724  -10.3125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -9.9000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -9.0750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -4.1250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -3.7125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -2.8875    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
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  2  0  0  0  0
  9  8  1  4  0  0  0
  9 10  2  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 14 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 15 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 21  2  0  0  0  0
 12 21  1  0  0  0  0
  6 22  1  0  0  0  0
 22 23  2  0  0  0  0
  3 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0155037

> <DATABASE_NAME>
NP-MRD

> <SMILES>
COC1=CC=C(\C=N\N=C(O)C2=CC=C(OC)C(OC)=C2)C=C1OC

> <INCHI_IDENTIFIER>
InChI=1S/C18H20N2O5/c1-22-14-7-5-12(9-16(14)24-3)11-19-20-18(21)13-6-8-15(23-2)17(10-13)25-4/h5-11H,1-4H3,(H,20,21)/b19-11+

> <INCHI_KEY>
NMAFOTFIMHUMSK-YBFXNURJSA-N

> <FORMULA>
C18H20N2O5

> <MOLECULAR_WEIGHT>
344.367

> <EXACT_MASS>
344.137221752

> <JCHEM_ACCEPTOR_COUNT>
7

> <JCHEM_ATOM_COUNT>
45

> <JCHEM_AVERAGE_POLARIZABILITY>
36.07364451482825

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
N-[(1E)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzene-1-carbohydrazonic acid

> <ALOGPS_LOGP>
3.04

> <JCHEM_LOGP>
2.754653808

> <ALOGPS_LOGS>
-4.63

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
7.36452817396657

> <JCHEM_PKA_STRONGEST_BASIC>
-2.989920786830293

> <JCHEM_POLAR_SURFACE_AREA>
81.87000000000002

> <JCHEM_REFRACTIVITY>
94.61000000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
8.11e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
N-[(1E)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 02-SEP-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   02-SEP-22         0                                  
HETATM    1  C   UNK     0      -2.667  -4.620   0.000  0.00  0.00           C+0
HETATM    2  O   UNK     0      -1.334  -5.390   0.000  0.00  0.00           O+0
HETATM    3  C   UNK     0      -1.334  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.000  -7.700   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.000  -9.240   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.334 -10.010   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -1.334 -11.550   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -2.667 -12.320   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0      -2.667 -13.860   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -4.001 -14.630   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -5.335 -13.860   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0      -4.001 -16.170   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.667 -16.940   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -2.667 -18.480   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -4.001 -19.250   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      -4.001 -20.790   0.000  0.00  0.00           O+0
HETATM   17  C   UNK     0      -2.667 -21.560   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -5.335 -18.480   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -6.668 -19.250   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -8.002 -18.480   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -5.335 -16.940   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.667  -9.240   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -2.667  -7.700   0.000  0.00  0.00           C+0
HETATM   24  O   UNK     0      -4.001  -6.930   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0      -4.001  -5.390   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4   23                                                  
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   22                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   21                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   18                                                  
CONECT   16   15   17                                                       
CONECT   17   16                                                            
CONECT   18   15   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19                                                            
CONECT   21   18   12                                                       
CONECT   22    6   23                                                       
CONECT   23   22    3   24                                                  
CONECT   24   23   25                                                       
CONECT   25   24                                                            
MASTER        0    0    0    0    0    0    0    0   25    0   52    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₈H₂₀N₂O₅

Average Mass

344.3670 Da

Monoisotopic Mass

344.13722 Da

IUPAC Name

N-[(1E)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzene-1-carbohydrazonic acid

Traditional Name

N-[(1E)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid

CAS Registry Number

Not Available

SMILES

COC1=CC=C(\C=N\N=C(O)C2=CC=C(OC)C(OC)=C2)C=C1OC

InChI Identifier

InChI=1S/C18H20N2O5/c1-22-14-7-5-12(9-16(14)24-3)11-19-20-18(21)13-6-8-15(23-2)17(10-13)25-4/h5-11H,1-4H3,(H,20,21)/b19-11+

InChI Key

NMAFOTFIMHUMSK-YBFXNURJSA-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
Melanthera biflora	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dimethoxybenzenes. These are organic aromatic compounds containing a monocyclic benzene moiety carrying exactly two methoxy groups.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Methoxybenzenes

Direct Parent

Dimethoxybenzenes

Alternative Parents

Substituents

Dimethoxybenzene
O-dimethoxybenzene
Benzoic acid or derivatives
Anisole
Benzoyl
Phenol ether
Phenoxy compound
Alkyl aryl ether
Ether
Carboxylic acid derivative
Organic nitrogen compound
Organooxygen compound
Organonitrogen compound
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Aromatic homomonocyclic compound

Molecular Framework

Aromatic homomonocyclic 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	3.04	ALOGPS
logP	2.75	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	7.36	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	7	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	81.87 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	94.61 m³·mol⁻¹	ChemAxon
Polarizability	36.07 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

5281771

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

6898813

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid (NP0155037)

MOL for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

3D MOL for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

3D SDF for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

3D-SDF for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

PDB for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

3D PDB for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

SMILES for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

INCHI for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

Structure for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)

3D Structure for NP0155037 (n-[(e)-(3,4-dimethoxyphenyl)methylidene]-3,4-dimethoxybenzenecarbohydrazonic acid)