1217669-02-7

Basic information

• Product Name: FMoc-(S)-3-AMino-5-hexynoic acid
• Synonyms: (9H-Fluoren-9-yl)MethOxy]Carbonyl (S)-3-Amino-5-hexynoic acid
• CAS NO: 1217669-02-7
• Molecular Formula: C21H19NO4
• Molecular Weight: 349.37986
• Mol File: 1217669-02-7.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: FMoc-(S)-3-AMino-5-hexynoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: FMoc-(S)-3-AMino-5-hexynoic acid(1217669-02-7)
• EPA Substance Registry System: FMoc-(S)-3-AMino-5-hexynoic acid(1217669-02-7)

Safety Data

• Hazardous Substances Data: 1217669-02-7(Hazardous Substances Data)

Upstream product

• 1417532-33-2 (S)-(9H-fluoren-9-yl)methyl (1-diazo-2-oxohex-5-yn-3-yl)carbamate 
• 23235-01-0 (2S)-2-amino-4-pentynoic acid 
• 82911-69-1 N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide 
• 198561-07-8 Fmoc-L-propargyl-Gly-OH 

Relevant articles and documents

Azide- and alkyne-functionalised α- And β3-amino acids

The synthesis and full characterisation of bifunctional β3-amino acids that have side chains functionalised with terminal azides (S)-4 and (R)-4 or acetylenes 5 and 6 is reported for the first time. The building blocks incorporate a turn-inducing β3-segment and a side chain that can be functionalised further, for example, through copper-catalysed Huisgen cycloaddition. Moreover, the corresponding α-amino acids 1 and 3 have been synthesised and characterised. All amino acid building blocks were of high optical purity as demonstrated by derivatisation and subsequent NMR analysis.