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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
Quality Level
assay
99%
form
crystals
mp
198-200 °C (lit.)
SMILES string
OC(=O)c1ccc(cc1)C(=O)c2ccccc2
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)
InChI key
IFQUPKAISSPFTE-UHFFFAOYSA-N
Gene Information
human ... ACHE(43), BCHE(590), CES1(1066)
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)
Regulatory Information
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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)
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
Synthesis and luminescent properties of terbium complex containing 4-benzoylbenzoic acid for application in NUV-based LED.
Naiqun S
Journal of Rare Earths, 34(2), 130-136 (2016)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| B12407-5G | 04061832492087 |
| B12407-25G | 04061833421611 |