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555398

Sigma-Aldrich

(4-Benzyloxy)phenylacetic acid

98%

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About This Item

Linear Formula:
C6H5CH2OC6H4CH2CO2H
CAS Number:
Molecular Weight:
242.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

119-123 °C (lit.)

functional group

carboxylic acid
phenyl

SMILES string

OC(=O)Cc1ccc(OCc2ccccc2)cc1

InChI

1S/C15H14O3/c16-15(17)10-12-6-8-14(9-7-12)18-11-13-4-2-1-3-5-13/h1-9H,10-11H2,(H,16,17)

InChI key

XJHGAJLIKDAOPE-UHFFFAOYSA-N

General description

(4-Benzyloxy)phenylacetic acid is a para-substituted phenyl-acetic acid derivative. Its crystals belong to the triclinic crystal system. Molecules of (4-benzyloxy)phenylacetic acid exists in centrosymmetric dimeric forms linked by double hydrogen bonds between carboxyl groups.

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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[4-(Benzyloxy) phenyl] acetic acid, C15H14O3.
Bats JW and Canenbley R.
Acta Crystallographica Section C, Crystal Structure Communications, 40(6), 993-995 (1984)
Crystallographic studies and physicochemical properties of Π-electron compounds. XVII. The structure of p-nitrophenylacetic acid.
Grabowski SJ, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 46(3), 428-430 (1990)
Tsung-I Hsu et al.
Oncotarget, 6(15), 13671-13687 (2015-04-25)
Herein, we evaluated the anti-cancer effect and molecular mechanisms of a novel betulinic acid (BA) derivative, SYK023, by using two mouse models of lung cancer driven by KrasG12D or EGFRL858R. We found that SYK023 inhibits lung tumor proliferation, without side

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