B12385
2-Benzoylbenzoic acid
98%
Sinónimos:
Benzophenone-2-carboxylic acid
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Fórmula lineal:
C6H5COC6H4CO2H
Número CAS:
Peso molecular:
226.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-612-2
Beilstein/REAXYS Number:
1107841
MDL number:
Assay:
98%
Form:
powder
Servicio técnico
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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
Clase de almacenamiento
11 - Combustible Solids
wgk
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