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Merck

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:
Peso molecular:
242.23
Beilstein/REAXYS Number:
2053625
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
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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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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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
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
Pierre Thuéry et al.
Dalton transactions (Cambridge, England : 2003), 49(3), 817-828 (2019-12-20)
Diphenic acid (H2dip) has been used to synthesize nine homo- or heterometallic uranyl ion complexes under solvo-hydrothermal conditions. The diphenate ligand dip2- adopts different coordination modes, mixtures of κ2-O,O'-chelation by individual carboxylate groups, chelation involving both carboxylate groups, and bridging
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
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

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