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Key Documents

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B12385

Sigma-Aldrich

2-Benzoylbenzoic acid

98%

Sinónimos:

Benzophenone-2-carboxylic acid

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About This Item

Fórmula lineal:
C6H5COC6H4CO2H
Número de CAS:
85-52-9
Peso molecular:
226.23
Beilstein/REAXYS Number:
1107841
EC Number:
201-612-2
MDL number:
MFCD00002472
UNSPSC Code:
12352100
PubChem Substance ID:
24891569
NACRES:
NA.22

assay

98%

form

powder

bp

257-265 °C (lit.)

mp

126-129 °C (lit.)

SMILES string

OC(=O)c1ccccc1C(=O)c2ccccc2

InChI

1S/C14H10O3/c15-13(10-6-2-1-3-7-10)11-8-4-5-9-12(11)14(16)17/h1-9H,(H,16,17)

Inchi Key

FGTYTUFKXYPTML-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Xiao Wang et al.
Organic letters, 13(4), 709-711 (2011-01-15)
2-Benzoylbenzoyl azides undergo facile cyclization under acidic conditions to give substituted dibenzo[b,f][1,5]-diazocines in good yields. This approach shortens the synthetic steps toward these compounds as compared with conventional methods. The mechanism of the diazocine synthesis is assumed to proceed by
Quentin Duez et al.
Polymers, 11(4) (2019-04-19)
Several families of polymers possessing various end-groups are characterized by ion mobility mass spectrometry (IMMS). A significant contribution of the end-groups to the ion collision cross section (CCS) is observed, although their role is neglected in current fitting models described
Marianne Placzek et al.
Acta dermato-venereologica, 93(1), 30-32 (2012-09-18)
Benzophenone is a phototoxic compound with absorption maxima in the ultraviolet A (UVA) and ultraviolet B (UVB) range. Many benzophenone derivatives are known to be photosensitizing. On the other hand, 2-hydroxy-4-methoxybenzophenone is used as a photoprotective agent. The aim of
Stanislav Gobec et al.
Bioorganic & medicinal chemistry letters, 15(23), 5170-5175 (2005-09-27)
Nonsteroidal anti-inflammatory drugs (NSAIDs) like indomethacin, flufenamic acid, and related compounds have been recently identified as potent inhibitors of AKR1C3. We report that some other NSAIDs (diclofenac and naproxen) also inhibit AKR1C3, with the IC(50) values in the low micromolar
Wojciech Ostrowski et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 967, 21-27 (2014-07-27)
Liquid chromatography coupled to mass spectrometry (MS) with electrospray ionization (ESI) is one of analytical techniques to obtain accurate results of low molecular weight aromatic compounds in biological samples of different origin. The interpretations of mass spectra of these aromatic

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