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Merck
CN

P16001

3-苯氧基丙酸

99%

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关于此项目

线性分子式:
C6H5OCH2CH2CO2H
化学文摘社编号:
分子量:
166.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
230-518-4
MDL number:
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产品名称

3-苯氧基丙酸, 99%

InChI key

BUSOTUQRURCMCM-UHFFFAOYSA-N

InChI

1S/C9H10O3/c10-9(11)6-7-12-8-4-2-1-3-5-8/h1-5H,6-7H2,(H,10,11)

SMILES string

OC(=O)CCOc1ccccc1

assay

99%

form

powder

bp

235-245 °C (lit.)

mp

98-100 °C (lit.)

Quality Level

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

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Luc M LeBlanc et al.
Rapid communications in mass spectrometry : RCM, 30(19), 2133-2144 (2016-08-02)
When subjected to collisional activation, gas-phase carboxylate ions typically undergo decarboxylation. However, alternative fragmentation processes dominate when the carboxylate group is located within certain structural motifs. In this work, the fragmentation processes of β-substituted carboxylate ions are characterized to improve
Wayne D Vaccaro et al.
Bioorganic & medicinal chemistry letters, 16(2), 395-399 (2005-10-26)
We report the discovery of novel histamine H(3) receptor antagonists based on 4-[(1H-imidazol-4-yl)methyl]piperidine. The most potent compounds in the series (e.g., 7) result from the attachment of a substituted aniline amide to the main pharmacophore piperidine via a two-methylene linker.

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