90427-70-6

Basic information

• Product Name: L-Alanine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-alanyl]-, phenylmethyl ester
• CAS NO: 90427-70-6
• Molecular Formula: C24H29N3O6
• Molecular Weight: 455.511
• Mol File: 90427-70-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-Alanine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-alanyl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-alanyl]-, phenylmethyl ester(90427-70-6)
• EPA Substance Registry System: L-Alanine, N-[N-[N-[(phenylmethoxy)carbonyl]-L-alanyl]-L-alanyl]-, phenylmethyl ester(90427-70-6)

Safety Data

• Hazardous Substances Data: 90427-70-6(Hazardous Substances Data)

Upstream product

• 2483-52-5 N-(N-benzyloxycarbonyl-L-alanyl)-D-alanine hydrazide 
• 2483-52-5 benzyl ((S)-1-(((S)-1-hydrazinyl-1-oxopropan-2-yl)amino)-1-oxopropan-2-yl)carbamate 
• 16012-70-7 benzyloxycarbonyl-L-alanyl-L-alanine 
• 17831-01-5 H-Ala-OBzl 

Downstream Products

• 5874-90-8 L-ala-L-ala-L-ala 

Relevant articles and documents

Small peptides as modular catalysts for the direct asymmetric aldol reaction: Ancient peptides with aldolase enzyme activity

Simple peptides and their analogues having a primary amino group as the catalytic residue mediate the direct asymmetric intermolecular aldol reaction with high stereoselectivity and furnish the corresponding aldol products with up to 99% ee; this intrinsic ability of highly modular peptides may explain the initial molecular evolution of aldolase enzymes. The Royal Society of Chemistry 2005.