B12385
2-Benzoylbenzoic acid
98%
Sinônimo(s):
Benzophenone-2-carboxylic acid
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About This Item
Produtos recomendados
Ensaio
98%
forma
powder
pb
257-265 °C (lit.)
pf
126-129 °C (lit.)
cadeia de caracteres SMILES
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)
chave InChI
FGTYTUFKXYPTML-UHFFFAOYSA-N
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Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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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
Polymers, 11(4) (2019-04-19)
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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
Bioorganic & medicinal chemistry letters, 15(23), 5170-5175 (2005-09-27)
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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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