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Merck
CN

136476

Sigma-Aldrich

2-(4-氟苯酰基)苯甲酸

97%

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线性分子式:
FC6H4COC6H4CO2H
CAS号:
分子量:
244.22
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

形式

solid

mp

138-140 °C (lit.)

SMILES字符串

OC(=O)c1ccccc1C(=O)c2ccc(F)cc2

InChI

1S/C14H9FO3/c15-10-7-5-9(6-8-10)13(16)11-3-1-2-4-12(11)14(17)18/h1-8H,(H,17,18)

InChI key

FJAZVXUPZQSZKI-UHFFFAOYSA-N

一般描述

2-(4-Fluorobenzoyl)benzoic acid on nitration with fuming HNO3 yields 2-(4-fluoro-3-nitrobenzoyl)benzoic acid.

应用

2-(4-Fluorobenzoyl)benzoic acid was used to prepare starting material for the synthesis of 9-fluoro-7H-benz(de)anthracene-7-one. It was used as starting reagent for the synthesis of Heparan sulfate glycosaminoglycans (HSGAG)-mimetic compounds.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)


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Keisuke Ishida et al.
Chemistry & biology, 11(3), 367-377 (2004-05-05)
Heparan sulfate glycosaminoglycans (HSGAGs) are involved in tumor cell growth, adhesion, invasion, and migration, due to their interactions with various proteins. In this study, novel HSGAG-mimetic compounds (KI compounds) were designed and synthesized. As a result of cell-based assays, KI-105
Active sites in dibenzopyrenes: Synthesis and studies of 3-fluoro-and 2, 10-difluorobenzo (RST) pentaphene.
Boger E, et al.
Journal of Fluorine Chemistry, 8(6), 513-525 (1976)

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