4-Hydroxyphenylacetic acid
Names | |
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IUPAC name
2-(4-Hydroxyphenyl)acetic acid | |
Other names
p-Hydroxyphenylacetic acid | |
Identifiers | |
156-38-7 | |
1448766 | |
ChEBI | CHEBI:18101 |
ChEMBL | ChEMBL1772 |
ChemSpider | 124 |
EC Number | 205-851-3 |
Jmol interactive 3D | Image |
PubChem | 127 |
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Properties | |
C8H8O3 | |
Molar mass | 152.15 g·mol−1 |
Appearance | Beige powder |
Melting point | 150 °C (302 °F; 423 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
4-Hydroxyphenylacetic acid is a chemical compound found in olive oil[1] and beer.[2] In industry the chemical is an intermediate used to synthesize atenolol[3] and 3,4-dihydroxyphenylacetic acid.[4]
Synthesis
4-Hydroxyphenylacetic acid is obtained by reducing 4-hydroxymandelic acid with elemental phosphorus and iodine.[3]
References
- ↑ Papadopoulos, George; Boskou, Dimitrios (1991). "Antioxidant effect of natural phenols on olive oil". Journal of the American Oil Chemists Society 68 (9): 669. doi:10.1007/BF02662292.
- ↑ Determination of free and bound phenolic acids in beer. M. Nardini and A. Ghiselli, Food Chemistry, January 2004, Volume 84, Issue 1, Pages 137–143, doi:10.1016/S0308-8146(03)00257-7
- 1 2 Mattioda, Georges and Christidis, Yani (2000). "Glyoxylic Acid". Ullmann's Encyclopedia of Industrial Chemistry: pg. 2. doi:10.1002/14356007.a12_495. Retrieved 27 December 2013.
- ↑ Sutton, Peter; Whittall, John; (2012). Practical Methods for Biocatalysis and Biotransformations 2. Chichester, West Sussex: John Wiley & Sons, Ltd. pp. 150–153. ISBN 9781119991397.
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