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
InChI key
XJHGAJLIKDAOPE-UHFFFAOYSA-N
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)
SMILES string
OC(=O)Cc1ccc(OCc2ccccc2)cc1
assay
98%
form
solid
mp
119-123 °C (lit.)
functional group
carboxylic acid, phenyl
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
新产品
此项目有
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)
[4-(Benzyloxy) phenyl] acetic acid, C15H14O3.
Bats JW and Canenbley R.
Acta Crystallographica Section C, Crystal Structure Communications, 40(6), 993-995 (1984)
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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