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126691

Sigma-Aldrich

Diphenic acid

97%

Sinónimos:

Biphenyl-2,2′-dicarboxylic acid

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About This Item

Fórmula lineal:
2-(HO2C)C6H4C6H4-2-(CO2H)
Número de CAS:
482-05-3
Peso molecular:
242.23
Beilstein/REAXYS Number:
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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Categorías relacionadas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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S Böhmer et al.
Biochemical and biophysical research communications, 244(1), 233-238 (1998-03-26)
Phenanthrene, a polycyclic aromatic hydrocarbon, was efficiently oxidized by laccase in the presence of both 1-hydroxybenzotriazole and unsaturated lipids. 73% of initially added phenanthrene was degraded within 182 hours to give phenanthrene-9,10-quinone and 2,2'-diphenic acid as the major products. The
[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)
[Effect of biphenyl dicarboxylate on abnormal laboratory findings in patients with chronic hepatitis and liver cirrhosis].
H Q Yu
Zhong xi yi jie he za zhi = Chinese journal of modern developments in traditional medicine, 3(3), 163-164 (1983-05-01)
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
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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