138372-38-0

Basic information

• Product Name: L-Leucine, N-[N-[N-[N-[O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- L-tyrosyl]glycyl]glycyl]-L-phenylalanyl]-, 1,1-dimethylethyl ester
• CAS NO: 138372-38-0
• Molecular Formula: C51H63N5O9
• Molecular Weight: 890.089
• Mol File: 138372-38-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-Leucine, N-[N-[N-[N-[O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- L-tyrosyl]glycyl]glycyl]-L-phenylalanyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Leucine, N-[N-[N-[N-[O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- L-tyrosyl]glycyl]glycyl]-L-phenylalanyl]-, 1,1-dimethylethyl ester(138372-38-0)
• EPA Substance Registry System: L-Leucine, N-[N-[N-[N-[O-(1,1-dimethylethyl)-N-[(9H-fluoren-9-ylmethoxy)carbonyl]- L-tyrosyl]glycyl]glycyl]-L-phenylalanyl]-, 1,1-dimethylethyl ester(138372-38-0)

Safety Data

• Hazardous Substances Data: 138372-38-0(Hazardous Substances Data)

Upstream product

• 89137-25-7 (S)-2-((S)-2-{2-[2-(9H-Fluoren-9-ylmethoxycarbonylamino)-acetylamino]-acetylamino}-3-phenyl-propionylamino)-4-methyl-pentanoic acid tert-butyl ester 
• 149204-99-9 Fmoc-Gly-L-Phe-L-Leu-OtBu 
• 84891-01-0 Fmoc-Phe-Leu-OtBu 
• 82362-19-4 Gly-Phe-Leu(t-Bu) 
• 28635-78-1 L-phenylalanyl-L-leucine tert-butyl ester 
• 2748-02-9 L-leucine tert-butyl ester hydrochloride 
• 35661-40-6 N-Fmoc L-Phe 
• 29022-11-5 N-(fluoren-9-ylmethoxycarbonyl)glycine 
• 71989-38-3 Fmoc-Tyr(tBu)-OH 
• 760-84-9 L-leucine hydrochloride 
• 77426-98-3 Gly-Gly-Phe-Leu-OBu^t 
• 139448-95-6 Fmoc-Tyr(Bu^t)-SH 

Downstream Products

• 81678-16-2 leucine enkephalin acetate 
• 427881-22-9 (S)-2-[(S)-2-(2-{2-[(S)-2-Amino-3-(4-tert-butoxy-phenyl)-propionylamino]-acetylamino}-acetylamino)-3-phenyl-propionylamino]-4-methyl-pentanoic acid tert-butyl ester 

Relevant articles and documents

Carbocations in action. Design, synthesis, and evaluation of a highly acid-sensitive naphthalene-based backbone amide linker for solid-phase synthesis

(Diagram presented) The design, synthesis, and properties of an extremely acid-labile backbone amide linker based on a regiospecifically substituted tetraalkoxy naphthaldehyde core are presented. This handle enables cleavage of peptide backbone amides (se

Formation of Peptide Thioamides by Use of Fmoc Amino Monothioacids and by PyBOP

Endothiopeptides have been obtained by using PyBOP promoted coupling between Fmoc-protected amino monothioacids and amino acid or peptide esters.The protected endothiopeptides (Fmoc-Gly-Φ(CSNH)-Phe-OEt, Fmoc-Tyr(But)-Φ(CSNH)-Gly-Gly-Phe-Leu-