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Key Documents

261793

Sigma-Aldrich

3-Benzoylbenzoic acid

99%

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About This Item

Linear Formula:
C6H5COC6H4CO2H
CAS Number:
Molecular Weight:
226.23
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

powder

mp

164-166 °C (lit.)

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

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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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.
Synthesis of flavonol derivatives as probes of biological processes.
Tanaka H, et al.
Tetrahedron Letters, 41(50), 9735-9739 (2000)
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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