NP-MRD: Showing NP-Card for 4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate (NP0148763)

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Record Information

Version

2.0

Created at

2022-09-02 04:33:31 UTC

Updated at

2022-09-02 04:33:31 UTC

NP-MRD ID

NP0148763

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate

Description

Biphenyl-4,4'-dicarboxylic acid diheptyl ester belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond. 4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate is found in Salvia multicaulis. Based on a literature review very few articles have been published on Biphenyl-4,4'-dicarboxylic acid diheptyl ester.

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1652309022206332D          

 32 33  0  0  0  0            999 V2000
   -7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -4.5375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013   -1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.8250    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0013    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5724    0.4125    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
   -2.8579    1.6500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289    1.6500    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
   -0.7145    2.8875    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    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   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    2.8875    0.0000 C   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    2.8875    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
    5.0013    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7158    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4302    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.6500    0.0000 C   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
   -2.1434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8579   -0.0000    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  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  0  0  0  0
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  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
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 25 26  1  0  0  0  0
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 29 30  2  0  0  0  0
 15 30  1  0  0  0  0
 14 31  1  0  0  0  0
 31 32  2  0  0  0  0
 11 32  1  0  0  0  0
M  END

     RDKit          3D

 70 71  0  0  0  0  0  0  0  0999 V2000
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   -2.6816   -2.3248    0.0419 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4889   -1.2433   -0.1677 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9488   -1.3657   -0.2025 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.1554   -0.3174   -0.4559 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6936   -0.8019    0.8569 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1956   -0.8861    0.8605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7766    0.4741    0.5993 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2950    0.3513    0.6282 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.9384    1.6986    0.3696 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5392    2.2498   -0.9803 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8826   -0.0131   -0.3472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4935    0.1054   -0.3129 C   0  0  0  0  0  0  0  0  0  0  0  0
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   12.7233    2.6586   -0.3042 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.0999    2.9348    0.3268 H   0  0  0  0  0  0  0  0  0  0  0  0
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   11.5089   -0.5430   -0.9879 H   0  0  0  0  0  0  0  0  0  0  0  0
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    9.2919    1.6623   -0.2826 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.4173   -0.4766   -1.3236 H   0  0  0  0  0  0  0  0  0  0  0  0
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    7.3329   -0.1870    1.2245 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2725    1.1945    0.7606 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7743    1.0774    0.7152 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.1321   -3.3175    0.1881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4694    0.7495   -0.5873 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4992   -0.9068   -1.3255 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2324   -1.7413    1.2251 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.3739   -0.0272    1.6190 H   0  0  0  0  0  0  0  0  0  0  0  0
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 30 15  1  0
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 28 66  1  0
M  END


  Mrv1652309022206332D          

 32 33  0  0  0  0            999 V2000
   -7.1447   -4.9500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -6.4302   -3.7125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7158   -3.3000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -5.0013   -2.0625    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.4289    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    0.0000    2.4750    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    2.8875    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    3.7125    0.0000 O   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    2.8875    0.0000 C   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    2.8875    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
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M  END
> <DATABASE_ID>
NP0148763

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCOC(=O)C1=CC=C(C=C1)C1=CC=C(C=C1)C(=O)OCCCCCCC

> <INCHI_IDENTIFIER>
InChI=1S/C28H38O4/c1-3-5-7-9-11-21-31-27(29)25-17-13-23(14-18-25)24-15-19-26(20-16-24)28(30)32-22-12-10-8-6-4-2/h13-20H,3-12,21-22H2,1-2H3

> <INCHI_KEY>
FZHRFXVOMMSJKS-UHFFFAOYSA-N

> <FORMULA>
C28H38O4

> <MOLECULAR_WEIGHT>
438.608

> <EXACT_MASS>
438.277009704

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
70

> <JCHEM_AVERAGE_POLARIZABILITY>
55.237758552757455

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate

> <ALOGPS_LOGP>
8.47

> <JCHEM_LOGP>
8.942635125333332

> <ALOGPS_LOGS>
-7.43

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-6.590049219890366

> <JCHEM_POLAR_SURFACE_AREA>
52.60000000000001

> <JCHEM_REFRACTIVITY>
130.59799999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
17

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.64e-05 g/l

> <JCHEM_TRADITIONAL_IUPAC>
4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate

> <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     -13.337  -9.240   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0     -12.003  -8.470   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0     -12.003  -6.930   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0     -10.669  -6.160   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0     -10.669  -4.620   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -9.336  -3.850   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      -9.336  -2.310   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      -8.002  -1.540   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0      -8.002  -0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0      -9.336   0.770   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0      -6.668   0.770   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      -6.668   2.310   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -5.335   3.080   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      -4.001   2.310   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -2.667   3.080   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -2.667   4.620   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -1.334   5.390   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.000   4.620   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   5.390   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       1.334   6.930   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       2.667   4.620   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.001   5.390   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       5.335   4.620   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       6.668   5.390   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       8.002   4.620   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       9.336   5.390   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      10.669   4.620   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.003   5.390   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       0.000   3.080   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      -1.334   2.310   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      -4.001   0.770   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      -5.335  -0.000   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12   32                                                  
CONECT   12   11   13                                                       
CONECT   13   12   14                                                       
CONECT   14   13   15   31                                                  
CONECT   15   14   16   30                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   29                                                  
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24                                                       
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28                                                       
CONECT   28   27                                                            
CONECT   29   18   30                                                       
CONECT   30   29   15                                                       
CONECT   31   14   32                                                       
CONECT   32   31   11                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   66    0
END

View in JSmol

Synonyms

Value	Source
Biphenyl-4,4'-dicarboxylate diheptyl ester	Generator

Chemical Formula

C₂₈H₃₈O₄

Average Mass

438.6080 Da

Monoisotopic Mass

438.27701 Da

IUPAC Name

4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate

Traditional Name

4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate

CAS Registry Number

Not Available

SMILES

CCCCCCCOC(=O)C1=CC=C(C=C1)C1=CC=C(C=C1)C(=O)OCCCCCCC

InChI Identifier

InChI=1S/C28H38O4/c1-3-5-7-9-11-21-31-27(29)25-17-13-23(14-18-25)24-15-19-26(20-16-24)28(30)32-22-12-10-8-6-4-2/h13-20H,3-12,21-22H2,1-2H3

InChI Key

FZHRFXVOMMSJKS-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
Salvia multicaulis	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond.

Kingdom

Organic compounds

Super Class

Benzenoids

Class

Benzene and substituted derivatives

Sub Class

Biphenyls and derivatives

Direct Parent

Biphenyls and derivatives

Alternative Parents

Substituents

Biphenyl
Benzoate ester
Benzoic acid or derivatives
Benzoyl
Dicarboxylic acid or derivatives
Carboxylic acid ester
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen 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	8.47	ALOGPS
logP	8.94	ChemAxon
logS	-7.4	ALOGPS
pKa (Strongest Basic)	-6.6	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	17	ChemAxon
Refractivity	130.6 m³·mol⁻¹	ChemAxon
Polarizability	55.24 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

15378965

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate (NP0148763)

MOL for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

3D MOL for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

3D SDF for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

3D-SDF for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

PDB for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

3D PDB for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

SMILES for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

INCHI for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

Structure for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)

3D Structure for NP0148763 (4,4'-diheptyl [1,1'-biphenyl]-4,4'-dicarboxylate)