123228-25-1

Basic information

• Product Name: N-tert-Butyloxycarbonyl-L-phenylalanyl-L-serine ethyl ester
• Synonyms: N-tert-Butyloxycarbonyl-L-phenylalanyl-L-serine ethyl ester
• CAS NO: 123228-25-1
• Molecular Weight: 380.441
• Mol File: 123228-25-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: N-tert-Butyloxycarbonyl-L-phenylalanyl-L-serine ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: N-tert-Butyloxycarbonyl-L-phenylalanyl-L-serine ethyl ester(123228-25-1)
• EPA Substance Registry System: N-tert-Butyloxycarbonyl-L-phenylalanyl-L-serine ethyl ester(123228-25-1)

Safety Data

• Hazardous Substances Data: 123228-25-1(Hazardous Substances Data)

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 26348-61-8 L-serine ethyl ester hydrochloride 
• 4117-31-1 ethyl L-serinate 

Downstream Products

• 271581-18-1 N-Benzyl-(N-tert-butyloxycarbonyl-L-phenylalanyl-DL-α-acetoxy)glycinamide 
• 271581-17-0 N-Benzyl-(N-tert-butyloxycarbonyl-L-phenylalanyl)-L-serinamide 
• 123228-32-0 (S)-2-((S)-2-(((tert-butoxy)carbonyl)amino)-3-phenylpropanamido)-3-hydroxypropanoic acid 

Relevant articles and documents

Biomimetic peptide bond formation in water with aminoacyl phosphate esters

Aminoacyl phosphates, biomimetic analogues of aminoacyl adenylates, react efficiently with amino acid esters to form dipeptides with retention of stereochemical integrity. The reactions are selective and occur readily in the presence of nucleophiles other than amino groups on their side chains. Aminoacyl phosphate esters that lack an amino-protecting group are also suitable for peptide bond formation, leading to a simplified overall process.