261793
3-Benzoylbenzoic acid
99%
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About This Item
Linear Formula:
C6H5COC6H4CO2H
CAS Number:
Molecular Weight:
226.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
powder
Quality Level
InChI
1S/C14H10O3/c15-13(10-5-2-1-3-6-10)11-7-4-8-12(9-11)14(16)17/h1-9H,(H,16,17)
SMILES string
OC(=O)c1cccc(c1)C(=O)c2ccccc2
InChI key
AXJXRLHTQQONQR-UHFFFAOYSA-N
assay
99%
form
powder
mp
164-166 °C (lit.)
functional group
carboxylic acid, ketone, phenyl
Related Categories
Application
3-Benzoylbenzoic acid has been used in:
- light-induced reactions on benzophenone-terminated boron-doped diamond (BDD) surfaces
- preparation of benzophenone flavonol derivative
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Synthesis of flavonol derivatives as probes of biological processes.
Tanaka H, et al.
Tetrahedron Letters, 41(50), 9735-9739 (2000)
Sabine Szunerits et al.
Chemical communications (Cambridge, England), (27)(27), 2793-2795 (2007-07-05)
Irradiation of a patterned benzophenone-terminated boron-doped diamond (BDD) surface with UV light (lambda = 350 nm) in the presence of a 15(mer) oligonucleotide resulted in the covalent linking of the DNA strand to the BDD interface.
Marta T Ignasiak et al.
The journal of physical chemistry. B, 118(29), 8549-8558 (2014-06-20)
The Met residue oxidation has been studied for decades. Although many efforts have been made on the identification of free radicals, some doubts remain about their final fates, i.e., the nature of stable oxidation products. The photosensitized oxidation processes of
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