(R)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid

• CAT Number: R073565
• CAS Number: 63039-46-3
• Molecular Formula: C10H15NO4
• Molecular Weight: 213.23
• Purity: ≥95%
• Synonyms: (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]pent-4-ynoic acid
• InChI: InChI=1S/C10H15NO4/c1-5-6-7(8(12)13)11-9(14)15-10(2,3)4/h1,7H,6H2,2-4H3,(H,11,14)(H,12,13)/t7-/m1/s1
• InChIKey: AMKHAJIFPHJYMH-SSDOTTSWSA-N
• SMILES: CC(C)(C)OC(=O)NC(CC#C)C(=O)O

(R)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid is a Glycine (HY-Y0966) derivative[1]. (R)-2-((tert-Butoxycarbonyl)amino)pent-4-ynoic acid is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

Reference

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.
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