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About This Item
Linear Formula:
FC6H4COC6H4CO2H
CAS Number:
Molecular Weight:
244.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay
97%
form
solid
mp
138-140 °C (lit.)
SMILES string
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
General description
2-(4-Fluorobenzoyl)benzoic acid on nitration with fuming HNO3 yields 2-(4-fluoro-3-nitrobenzoyl)benzoic acid.
Application
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.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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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