75779-22-5

Basic information

• Product Name: H-Leu-Ala-OH
• CAS NO: 75779-22-5
• Molecular Weight: 292.378
• Mol File: 75779-22-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: H-Leu-Ala-OH(CAS DataBase Reference)
• NIST Chemistry Reference: H-Leu-Ala-OH(75779-22-5)
• EPA Substance Registry System: H-Leu-Ala-OH(75779-22-5)

Safety Data

• Hazardous Substances Data: 75779-22-5(Hazardous Substances Data)

Upstream product

• 17664-94-7 N-(benzyloxycarbonyl)-L-leucyl-L-alanine phenylmethyl ester 
• 42854-62-6 L-alanine benzyl ester p-toluenesulfonate 
• 3190-70-3 L-leucine N-carboxyanhydride 
• 66415-01-8 N-((tert-butoxycarbonyl)-L-leucyl)-L-alanine benzyl ester 
• 13139-15-6 N-tert-butoxycarbonyl-L-leucine 
• 17831-01-5 H-Ala-OBzl 
• 100-39-0 benzyl bromide 
• 126400-95-1 N-(tert-butoxycarbonyl)-L-alanine benzyl ester 
• 66450-17-7 Boc-Leu-HONB 

Downstream Products

• 7298-84-2 Leu-Ala 

Relevant articles and documents

Design criteria for minimalist mimics of protein-protein interface segments

Small molecules that can interrupt or inhibit protein-protein interactions (PPIs) are valuable as probes in chemical biology and medicinal chemistry, but they are also notoriously difficult to develop. Design of non-peptidic small molecules that mimic ami

Application of a unique automated synthesis system for solution-phase peptide synthesis

An automated synthesis system, which is suitable for repetitive syntheses using similar reaction procedures, was used to synthesize systematically a library of all possible dipeptides (25) and tripeptides (125) from 5 protected amino acids. The apparatus has also been applied to the automated synthesis of 10 fragment tripeptide derivatives that are constituents of the hormone PACAP-27. The measured molecular optical rotation values of the library of 125 tripeptides were found to correlate well with calculated values obtained by summation of the molecular optical rotation values for the constituent amino acids.