About This Item
Fórmula linear:
C6H5CH2OC6H4CO2H
Número CAS:
Peso molecular:
228.24
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
99%
pf
189-192 °C (lit.)
grupo funcional
carboxylic acid
phenyl
cadeia de caracteres SMILES
OC(=O)c1ccc(OCc2ccccc2)cc1
InChI
1S/C14H12O3/c15-14(16)12-6-8-13(9-7-12)17-10-11-4-2-1-3-5-11/h1-9H,10H2,(H,15,16)
chave InChI
AQSCHALQLXXKKC-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
4-Benzyloxybenzoic acid is a substituted benzoic acid that can be prepared by the benzylation of 4-hydroxybenzoic acid with benzyl bromide.
Aplicação
4-Benzyloxybenzoic acid may be used in the preparation of 1,3-phenylene bis(4-benzyloxybenzoate). It may also be used in the preparation of (-)-(2R,3R)-5,7-bis(benzyloxy)-2-[3,4,5-tris(benzyloxy)-phenyl]chroman-3-yl-(4-benzyloxy)benzoate.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - Eye Irrit. 2
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
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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Synthesis and characterization of achiral banana-shaped liquid crystalline molecules containing bisnaphthyl moieties.
Yang PJ and Lin HC.
Liq. Cryst., 33(5), 587-603 (2006)
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Acta poloniae pharmaceutica, 60(6), 477-480 (2004-04-15)
A series of alkanolamides have been tested for anticonvulsant activity in the maximal electroshock seizure (MES) and subcutaneous pentylenetetrazole seizure treshold (ScMet) assays and for neurotoxicity (TOX) in rodents. Most interesting were the anticonvulsant results of 2N-methylaminoethanol derivative II, which
Kumi Osanai et al.
Tetrahedron, 63(32), 7565-7570 (2007-08-06)
The total and semi syntheses of (2R, 3R)-epigallocatechin-3-O-(4-hydroxybenzoate), a novel catechin from Cistus salvifolius, was accomplished. The proteasome inhibition and cytotoxic activities of the synthetic compound and its acetyl derivative were studied and compared with (2R, 3R)-epigallocatechin-3-gallate (EGCG), the active
Semi-synthesis and proteasome inhibition of D-ring deoxy analogs of (-)-epigallocatechin gallate (EGCG), the active ingredient of green tea extract.
Huo C, et al.
Canadian Journal of Chemistry, 86(6), 495-502 (2008)
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