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Merck
CN

555398

4-苄氧基苯乙酸

98%

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关于此项目

线性分子式:
C6H5CH2OC6H4CH2CO2H
化学文摘社编号:
分子量:
242.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
229-463-9
MDL number:
Assay:
98%
Form:
solid
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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.


存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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分析证书(COA)

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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



全球贸易项目编号

货号GTIN
555398-1G04061825586120
555398-5G04061831821291