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261793

Sigma-Aldrich

3-Benzoylbenzoic acid

99%

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About This Item

Linear Formula:
C6H5COC6H4CO2H
CAS Number:
579-18-0
Molecular Weight:
226.23
MDL number:
MFCD00002518
UNSPSC Code:
12352100
PubChem Substance ID:
24855834
NACRES:
NA.22

assay

99%

form

powder

mp

164-166 °C (lit.)

functional group

carboxylic acid

SMILES string

OC(=O)c1cccc(c1)C(=O)c2ccccc2

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)

InChI key

AXJXRLHTQQONQR-UHFFFAOYSA-N

Application

3-Benzoylbenzoic acid has been used in:
  • light-induced reactions on benzophenone-terminated boron-doped diamond (BDD) surfaces
  • preparation of benzophenone flavonol derivative

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK5081
STBJ9052
STBF2993V
STBD1442V
STBB5231V

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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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