3-(2-羟苯基)丙酸
3-(2-羟苯基)丙酸结构式
|
常用名 | 3-(2-羟苯基)丙酸 | 英文名 | 3-(2-Hydroxyphenyl)propionate |
|---|---|---|---|---|
| CAS号 | 495-78-3 | 分子量 | 166.174 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 335.9±17.0 °C at 760 mmHg | |
| 分子式 | C9H10O3 | 熔点 | 86-89 °C(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 171.2±17.4 °C | |
| 符号 |
GHS07 |
信号词 | Warning |
|
Catabolism of phenylpropionic acid and its 3-hydroxy derivative by Escherichia coli.
J. Bacteriol. 155(1) , 113-121, (1983) A number of laboratory strains and clinical isolates of Escherichia coli utilized several aromatic acids as sole sources of carbon for growth. E. coli K-12 used separate reactions to convert 3-phenylpropionic and 3-(3-hydroxyphenyl)propionic acids into 3-(2,3... |
|
|
Constituents of Justicia pectoralis Jacq. 2. Gas chromatography/mass spectrometry of simple coumarins, 3-phenylpropionic acids and their hydroxy and methoxy derivatives.
Biomed. Environ. Mass Spectrom. 15(8) , 413-417, (1988) The analysis of extracts from the South American plant Justicia pectoralis Jacq. permitted the identification, among other compounds, of coumarin, dihydrocoumarin, umbelliferone and 3-(2-hydroxyphenyl)propionic acid by gas chromatography/mass spectrometry (GC... |
|
|
Antiulcerogenic compounds isolated from Chinese cinnamon.
Planta Med. 55(3) , 245-248, (1989) Two active compounds that prevent serotonin-induced ulcerogenesis in rats were isolated from Chinese cinnamon (the stem bark of Cinnamomum cassia) and identified as 3-(2-hydroxyphenyl)-propanoic acid and its O-glucoside. The former compound, administered oral... |
|
|
Microbial metabolism of catechin stereoisomers by human faecal microbiota: comparison of targeted analysis and a non-targeted metabolomics method. Aura AM, et al.
Phytochem. Lett. 1(1) , 18-22, (2008)
|
|
|
Structure of 3-(2-hydroxyphenyl) propionic acid. Begum NS, et al.
Acta Crystallogr. C 48(6) , 1076-1078, (1992)
|