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About This Item
Linear Formula:
C6H5COC6H4CO2H
CAS Number:
Molecular Weight:
226.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-286-0
Beilstein/REAXYS Number:
1960224
MDL number:
Assay:
99%
Form:
crystals
InChI key
IFQUPKAISSPFTE-UHFFFAOYSA-N
InChI
1S/C14H10O3/c15-13(10-4-2-1-3-5-10)11-6-8-12(9-7-11)14(16)17/h1-9H,(H,16,17)
SMILES string
OC(=O)c1ccc(cc1)C(=O)c2ccccc2
assay
99%
form
crystals
Quality Level
Gene Information
human ... ACHE(43), BCHE(590), CES1(1066)
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General description
4-Benzoylbenzoic acid is a benzophenone derivative. It can undergo hydrogenolysis to 4-benzylbenzoic acid. Cotton fabrics incorporated with 4-benzoylbenzoic acid have shown pesticide degradation ability, when exposed to UV irradiation.
Application
4-Benzoylbenzoic acid, along with methacrylic acid can be used as ligands for synthesizing a novel Tb(III) ternary complex with luminescent property.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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3-Mercapto-1, 2, 4-triazoles and N-acylated thiosemicarbazides as metallo-?-lactamase inhibitors.
Hussein W
Bioorganic & Medicinal Chemistry Letters, 22(1), 380-386 (2012)
K M Defife et al.
Journal of biomaterials science. Polymer edition, 10(10), 1063-1074 (1999-12-11)
Amphiphilic chains of 4-benzoylbenzoic acid moieties and polymer were photochemically immobilized onto silicone rubber to ask whether the covalently coupled polymers would passivate the silicone rubber by inhibiting protein adsorption and subsequent cell adhesion and activation. Three groups of polymers
K M DeFife et al.
Journal of biomedical materials research, 44(3), 298-307 (1999-07-09)
Photochemical immobilization technology was utilized to covalently couple polymers to silicone rubber either at multiple points along a polymer backbone or at the endpoint of an amphiphilic chain. The coating variants then were tested in vitro and in vivo for
Antimicrobial and chemical detoxifying functions of cotton fabrics containing different benzophenone derivatives.
Hong K
Carbohydrate Polymers, 71(4), 598-605 (2008)
G Scholz et al.
The Journal of biological chemistry, 264(8), 4318-4321 (1989-03-15)
4-Benzoylbenzoic acid inhibits pyridoxal kinase activity competitively with respect to pyridoxal. The Ki was determined to be 5 x 10(-5) M. Binding studies showed that 4-benzoylbenzoic acid bound to pyridoxal kinase at a 1:1 molar ratio and with a dissociation
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