6402-95-5

Basic information

• Product Name: L-Alanine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester
• CAS NO: 6402-95-5
• Molecular Formula: C21H24N2O6
• Molecular Weight: 400.431
• Mol File: 6402-95-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: L-Alanine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester(6402-95-5)
• EPA Substance Registry System: L-Alanine, N-[N-[(phenylmethoxy)carbonyl]-L-seryl]-, phenylmethyl ester(6402-95-5)

Safety Data

• Hazardous Substances Data: 6402-95-5(Hazardous Substances Data)

Upstream product

• 17831-01-5 H-Ala-OBzl 
• 1145-80-8 N-(benzyloxycarbonyl)-L-serine 
• 42854-62-6 L-alanine benzyl ester p-toluenesulfonate 

Downstream Products

• 6403-17-4 L-ser-L-ala 

Relevant articles and documents

The small peptide-catalyzed direct asymmetric aldol reaction in water

The asymmetric aldol reaction is a powerful method for forming carbon-carbon bonds. Small peptides with a primary amine as the catalytic residue catalyze asymmetric aqueous aldol reactions between unmodified ketones and aldehydes to furnish the corresponding aldol products with high ees. The high momodularity of the small peptides should enable the construction of several novel catalysts by combinatorial techniques for the aqueous asymmetric aldol reaction. The remarkably high difference in stereoselectivity between the peptide bond-formation was an important step towards the evaluation of asymmetric catalysis and homochilarity.

Synthesis of phosphopeptides. V. Further dipeptides, tripeptides and O-phosphorylated derivatives of L-serine.

-