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Merck
CN

512354

4-Benzyloxybenzoic acid

99%

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About This Item

Linear Formula:
C6H5CH2OC6H4CO2H
CAS Number:
Molecular Weight:
228.24
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
216-066-0
MDL number:
Assay:
99%
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Quality Level

assay

99%

mp

189-192 °C (lit.)

functional group

carboxylic acid, phenyl

SMILES string

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)

InChI key

AQSCHALQLXXKKC-UHFFFAOYSA-N

General description

4-Benzyloxybenzoic acid is a substituted benzoic acid that can be prepared by the benzylation of 4-hydroxybenzoic acid with benzyl bromide.

Application

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.


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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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
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)
Henryk Marona et al.
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



Global Trade Item Number

SKUGTIN
512354-5G04061831830033