3-(2-Hydroxyphenyl)propionate
3-(2-Hydroxyphenyl)propionate structure
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Common Name | 3-(2-Hydroxyphenyl)propionate | ||
|---|---|---|---|---|
| CAS Number | 495-78-3 | Molecular Weight | 166.174 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 335.9±17.0 °C at 760 mmHg | |
| Molecular Formula | C9H10O3 | Melting Point | 86-89 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 171.2±17.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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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... |
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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... |
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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... |
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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)
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Structure of 3-(2-hydroxyphenyl) propionic acid. Begum NS, et al.
Acta Crystallogr. C 48(6) , 1076-1078, (1992)
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