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126691

Sigma-Aldrich

Diphenic acid

97%

Synonym(s):

Biphenyl-2,2′-dicarboxylic acid

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About This Item

Linear Formula:
2-(HO2C)C6H4C6H4-2-(CO2H)
CAS Number:
482-05-3
Molecular Weight:
242.23
Beilstein:
2053625
EC Number:
207-576-4
MDL number:
MFCD00002464
UNSPSC Code:
12162002
PubChem Substance ID:
24847739
NACRES:
NA.23

Assay

97%

mp

227-229 °C (lit.)

SMILES string

OC(=O)c1ccccc1-c2ccccc2C(O)=O

InChI

1S/C14H10O4/c15-13(16)11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(17)18/h1-8H,(H,15,16)(H,17,18)

InChI key

GWZCCUDJHOGOSO-UHFFFAOYSA-N

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Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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K E Hammel et al.
Applied and environmental microbiology, 58(6), 1832-1838 (1992-06-01)
The ligninolytic fungus Phanerochaete chrysosporium oxidized phenanthrene and phenanthrene-9,10-quinone (PQ) at their C-9 and C-10 positions to give a ring-fission product, 2,2'-diphenic acid (DPA), which was identified in chromatographic and isotope dilution experiments. DPA formation from phenanthrene was somewhat greater
F H Clarke et al.
Journal of pharmaceutical sciences, 76(8), 611-620 (1987-08-01)
A convenient procedure has been developed for the determination of partition and distribution coefficients. The method involves the potentiometric titration of the compound, first in water and then in a rapidly stirred mixture of water and octanol. An automatic titrator
Masashi Kunitake et al.
Langmuir : the ACS journal of surfaces and colloids, 21(20), 9206-9210 (2005-09-21)
Formation of adlayers of the optically active compound 1,1'-binaphthyl-2, 2'-dicarboxylic acid (BINAC) on iodine-modified Au (111) surfaces in perchloric acid was investigated by in situ scanning tunneling microscopy (STM). Highly ordered arrays formed on the surfaces via simple spontaneous adsorption
K A Ohemeng et al.
Journal of medicinal chemistry, 40(20), 3292-3296 (1997-11-05)
The synthesis and inhibitory activity against DNA gyrase of a series of diphenic acid monohydroxamides 4a-f are described. A protocol of two biological assays showed conclusively that inhibition occurs specifically at the DNA-DNA gyrase complex and is not attributable to
Ai-zhi Wu et al.
Guang pu xue yu guang pu fen xi = Guang pu, 24(4), 421-423 (2005-03-16)
The ligand diphenic acid has been synthesized and the corresponding complexes of transition metal Co, Ni and Mn with diphenic acid have been prepared and characterized by the elementary analysis, IR spectra and ultraviolet-visible spectra. The results of IR show
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