126691
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:
Molecular Weight:
242.23
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
207-576-4
Beilstein/REAXYS Number:
2053625
MDL number:
InChI key
GWZCCUDJHOGOSO-UHFFFAOYSA-N
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)
SMILES string
OC(=O)c1ccccc1-c2ccccc2C(O)=O
assay
97%
mp
227-229 °C (lit.)
Quality Level
Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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[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)
[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
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
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
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