Chemistry:4-Hydroxyphenylacetic acid
From HandWiki
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| Names | |
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| Preferred IUPAC name
(4-Hydroxyphenyl)acetic acid | |
| Other names
p-Hydroxyphenylacetic acid
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| Identifiers | |
3D model (JSmol)
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| 1448766 | |
| ChEBI | |
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PubChem CID
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| Properties | |
| C8H8O3 | |
| Molar mass | 152.149 g·mol−1 |
| Appearance | Beige powder |
| Melting point | 150 °C (302 °F; 423 K) |
| Hazards | |
| Safety data sheet | MSDS at Sigma Aldrich |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Tracking categories (test):
4-Hydroxyphenylacetic acid is a chemical compound found in olive oil[1] and beer.[2]
Synthesis
4-Hydroxyphenylacetic acid is obtained by reducing 4-hydroxymandelic acid with elemental phosphorus and iodine.[3]
Uses
In industry, 4-hydroxyphenylacetic acid is an intermediate used to synthesize atenolol,[3] 3,4-dihydroxyphenylacetic acid,[4] and coclaurine.
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
- ↑ 3.0 3.1 Mattioda, Georges; Christidis, Yani (2000). Glyoxylic Acid. 2. doi:10.1002/14356007.a12_495. ISBN 978-3527306732.
- ↑ Sutton, Peter; Whittall, John (2012). Practical Methods for Biocatalysis and Biotransformations 2. Chichester, West Sussex: John Wiley & Sons, Ltd.. pp. 150–153. ISBN 9781119991397. https://books.google.com/books?id=WlODZ-WX8vIC&q=9781119991397.
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