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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

Quality Level

100

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

Certificates of Analysis (COA)

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[The QSAR of diphenic acids in increasing macrophage phagocytosis].
R L Gu et al.
Hua xi yi ke da xue xue bao = Journal of West China University of Medical Sciences = Huaxi yike daxue xuebao, 17(3), 224-227 (1986-09-01)
Shinya Hirano et al.
Chemical communications (Cambridge, England), (5)(5), 643-644 (2005-01-27)
As a model for DNA damage by photodimerization of its thymine component, a new [2 + 2] photodimerization of 5-chloro and 5-methyl-2-pyridone to the corresponding cis-anti-dimers as their inclusion complexes with 1,1'-biphenyl-2,2'-dicarboxylic acid was found, and the mechanism of this
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
Xiang-Wen Kong et al.
Chemistry & biodiversity, 5(9), 1743-1752 (2008-09-26)
In search of novel anticancer agents, two series of dimethyl [1,1'-biphenyl]-2,2'-dicarboxylate derivatives, 8a-8k and 9a-9k, containing both methylenedioxy and 1,3,4-thiadiazole moieties were designed and synthesized. Cytotoxicity of these compounds was evaluated in vitro against five human tumor cell lines, i.e.
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
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