(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid

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(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid Basic information
Product Name:(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid
Synonyms:(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid;O-propargyltyrosine;H-D-Tyr(Propargyl)-OH;O-Propargyl-D-tyrosine;D-Tyrosine, O-2-propyn-1-yl-;(R)-2-Amino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid;2-amino-3-(2-fluoro-5-methyl-4-(trifluoromethyl)phenyl)propanoic acid
CAS:1170674-20-0
MF:C12H13NO3
MW:219.24
EINECS:
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Mol File:1170674-20-0.mol
(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid Structure
(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid Chemical Properties
Boiling point 395.988±42.00 °C(Press: 760.00 Torr)(predicted)
density 1.230±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka2.226±0.10(predicted)
Safety Information
MSDS Information
(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid Usage And Synthesis
UsesH-D-Tyr(Propargyl)-OH is a click chemistry reagent containing an Azide[1]. H-D-Tyr(Propargyl)-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
References[1] Nimmo ZM, et al. Development of optimized conditions for Glaser-Hay bioconjugations. Bioorg Chem. 2018 Feb;76:326-331. DOI:10.1016/j.bioorg.2017.11.020
(S)-2-aMino-3-(4-(prop-2-yn-1-yloxy)phenyl)propanoic acid Preparation Products And Raw materials
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