Chemistry:Tyrosinol
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Other names
β-amino-4-hydroxybenzenepropanol
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Identifiers | |
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3D model (JSmol)
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ChemSpider | |
PubChem CID
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CompTox Dashboard (EPA)
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Properties | |
C9H13NO2 | |
Molar mass | 167.208 g·mol−1 |
Appearance | white solid |
Melting point | 91.4–92.1 °C (196.5–197.8 °F; 364.5–365.2 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Tyrosinol is an organic compound with the formula HOC
6H
4CH
2CH(NH
2)CH
2OH. A colorless or white solid, it is produced by the reduction of the amino acid tyrosine with borane dimethylsulfide.[1] The compound, which is chiral, is an example of a 1,2-ethanolamine as well as a phenethylamine.[2]
Related compounds
- tyrosol, HOC
6H
4CH
2CH
2OH
References
- ↑ Phoon, Chee Wee; Abell, Chris (1998). "Solid Phase Aldol and Conjugate Addition Reactions Using Evans' Oxazolidinone Chiral Auxiliary". Tetrahedron Letters 39 (17): 2655–2658. doi:10.1016/S0040-4039(98)00230-5.
- ↑ Martin Ernst; Johann-Peter Melder; Franz Ingo Berger; Christian Koch (2022). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_001.pub2.
Original source: https://en.wikipedia.org/wiki/Tyrosinol.
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