71989-12-3

Basic information

• Product Name: N-<<(9-Fluorenylmethyl)oxy>carbonyl>-O-tert-butyl-L-tyrosyl-L-leucyl-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide
• Synonyms: N-<<(9-Fluorenylmethyl)oxy>carbonyl>-O-tert-butyl-L-tyrosyl-L-leucyl-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide
• CAS NO: 71989-12-3
• Molecular Weight: 1198.51
• Mol File: 71989-12-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-<<(9-Fluorenylmethyl)oxy>carbonyl>-O-tert-butyl-L-tyrosyl-L-leucyl-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-<<(9-Fluorenylmethyl)oxy>carbonyl>-O-tert-butyl-L-tyrosyl-L-leucyl-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide(71989-12-3)
• EPA Substance Registry System: N-<<(9-Fluorenylmethyl)oxy>carbonyl>-O-tert-butyl-L-tyrosyl-L-leucyl-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide(71989-12-3)

Safety Data

• Hazardous Substances Data: 71989-12-3(Hazardous Substances Data)

Upstream product

• 71989-10-1 <<(9-Fluorenylmethyl)oxy>carbonyl>-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide 
• 71989-09-8 N-<<(9-Fluorenylmethyl)oxy>carbonyl>-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide 
• 71989-34-9 Fmoc-Ser(t-Bu)-ONp 
• 71989-08-7 <(Benzyloxy)carbonyl>-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide 
• 71989-07-6 <(Benzyloxy)carbonyl>-L-valyl-L-leucyl-O-tert-butyl-L-threonine Methyl Ester 
• 71989-38-3 Fmoc-Tyr(tBu)-OH 
• 71989-33-8 Fmoc-Ser(tBu)-OH 
• 17708-79-1 (S)-2-((S)-2-(((benzyloxy)carbonyl)amino)-3-methylbutanamido)-4-methylpentanoic acid 
• 35661-60-0 Fmoc-Leu-OH 
• 10512-93-3 Z-Val-ONp 
• 61-90-5 L-leucine 
• 71989-39-4 Fmoc-Tyr(t-Bu)-ONp 
• 71989-11-2 <<(9-Fluorenylmethyl)oxy>carbonyl>-L-leucyl-L-asparaginyl-O-tert-butyl-L-seryl-L-valyl-L-leucyl-O-tert-butyl-L-threoninamide 

Relevant articles and documents

Active Esters of 9-Fluorenylmethyloxycarbonyl Amino Acids and Their Application in the Stepwise Lengthening of a Peptide Chain

Preparation and properties of p-nitrophenyl esters of several 9-fluorenylmethyloxycarbonyl (Fmoc) amino acids are described.The Fmoc derivatives of the hindered amino acids valine and isoleucine were converted to the more reactive o-nitrophenyl esters whi