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25 G
$212.00
100 G
$511.00
About This Item
线性分子式:
2-(HO2C)C6H4C6H4-2-(CO2H)
CAS号:
分子量:
242.23
Beilstein:
2053625
EC 号:
MDL编号:
UNSPSC代码:
12162002
PubChem化学物质编号:
NACRES:
NA.23
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质量水平
方案
97%
mp
227-229 °C (lit.)
SMILES字符串
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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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
其他客户在看
[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)
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
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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