82748-54-7

Basic information

• Product Name: L-Alanine, N-L-alanyl-, phenylmethyl ester
• CAS NO: 82748-54-7
• Molecular Formula: C13H18N2O3
• Molecular Weight: 250.298
• Mol File: 82748-54-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: L-Alanine, N-L-alanyl-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-L-alanyl-, phenylmethyl ester(82748-54-7)
• EPA Substance Registry System: L-Alanine, N-L-alanyl-, phenylmethyl ester(82748-54-7)

Safety Data

• Hazardous Substances Data: 82748-54-7(Hazardous Substances Data)

Upstream product

• 1948-31-8 di-L-alanine 
• 100-51-6 benzyl alcohol 
• 18670-98-9 N-(tert-butoxycarbonyl)-L-alanyl-L-alanine benzyl ester 
• 42854-62-6 L-alanine benzyl ester p-toluenesulfonate 
• 2224-52-4 L-alanine N-carboxyanhydride 

Downstream Products

• 74257-83-3 Boc-V-A-A-OCH₂Ph 
• 1242760-42-4 Boc-Gln-Ala-Ala-OCH₂Ph 
• 1242760-41-3 Boc-Ser-Ala-Ala-OCH₂Ph 
• 344908-22-1 Boc-F-A-A-OCH₂Ph 
• 1948-31-8 di-L-alanine 

Relevant articles and documents

Synthesis of novel D-α-galactopyranosyl-L-seryl/L-threonyl-L-alanyl-L-alanine as useful precursors of new glycopeptide antibiotics with computational calculations studies

New, simple, synthetic routes for the preparation of novel glycopeptide antibiotics are described. The structures of the synthesized compounds are elucidated by IR, two-dimensional NMR spectroscopy, and mass spectrometry. The stability of the new glycopep

The synthesis of pure Amadori rearrangement products

The term "Maillard reaction" is used to describe a complex set of reactions in foods leading to flavour generation and non-enzymatic browning.The first step in this process is the so-called Amadori rearrangement: a reducing saccharide and a peptide fragment react to form an Amadori Rearrangement Product (ARP).To be able to do model studies on flavour generation, gram amounts of pure ARP are required.In the present study, glucose-derived ARPs were synthesised from specifically protected and activated starting compounds.After deprotection and purification, pure ARPs were obtained.This is the first time that ARPs of dipeptides have been isolated.

[Asn2 ]-thymosin α1 and analogs thereof

Thymosin α1, was chemically synthesized by the fragment condensation of the protected amino terminal tetradecapeptide with the protected carboxyl terminal tetradecapeptide. Similarly prepared was the analog [Asn2 ]-thymosin α1 utilizing the appropriately modified protected amino terminal tetradecapeptide. Both products are active as agents which affect regulation, differentiation and function of thymus dependent lymphocytes (T cells).