13585-98-3

Basic information

• Product Name: L-Alanine, N-[(phenylmethoxy)carbonyl]-L-alanyl-L-alanyl-
• CAS NO: 13585-98-3
• Molecular Formula: C17H23N3O6
• Molecular Weight: 365.386
• Mol File: 13585-98-3.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: L-Alanine, N-[(phenylmethoxy)carbonyl]-L-alanyl-L-alanyl-(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-[(phenylmethoxy)carbonyl]-L-alanyl-L-alanyl-(13585-98-3)
• EPA Substance Registry System: L-Alanine, N-[(phenylmethoxy)carbonyl]-L-alanyl-L-alanyl-(13585-98-3)

Safety Data

• Hazardous Substances Data: 13585-98-3(Hazardous Substances Data)

Upstream product

• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 35661-39-3 N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-alanine 
• 41036-19-5 L-alanyl-alanine methylester hydrochloride 
• 19794-10-6 (S)-methyl 2-((S)-2-((tert-butoxycarbonyl)amino)propanamido)propanoate 
• 16012-70-7 benzyloxycarbonyl-L-alanyl-L-alanine 
• 76413-56-4 3-(N-benzyloxycarbonyl-L-alanyl)-1,3-thiazolidine-2-thione 
• 95930-17-9 L-Ala-L-Ala-OH*HBr 
• 13883-50-6 Z-(L-Ala)3-O-t-Bu 
• 3057-69-0 N-[(benzyloxy)carbonyl]-L-alanyl-L-alanyl-L-alanine methyl ester 

Downstream Products

• 95930-19-1 N^α-benzyloxycarbonyl-N^ε-t-butoxycarbonyl-L-lysyl-L-alanyl-L-alanyl-L-alanine 
• 90427-69-3 Glp-Ala₃-PheCH₃ 
• 90427-67-1 Ac-Ala₃-PheCH₃ 
• 5874-90-8 L-ala-L-ala-L-ala 
• 89595-83-5 Z-Ala₃-PheCH₂Cl 
• 88576-79-8 Z-Ala₂-Ala-PheCH₃ 
• 90427-62-6 Z-Ala₂-Ala-AlaCH₃ 
• 73974-15-9 6-(Benzyloxycarbonyl-alanyl-alanyl-alanylamino)penicillansaeure 

Relevant articles and documents

Methyl to trifluoromethyl substitution as a strategy to increase the membrane permeability of short peptides

Here, we investigated the effect of CH3to CF3substitution on the membrane permeability of peptides. We synthesized a series of peptides with CF3groups and corresponding nonfluorinated peptides and measured the membrane per

Peptide-bond Formation, Chemoselective Acylation of Amino Acids, and Crosslinking Reaction between Amino Acids Utilizing a Functional Five-membered Heterocycle, 1,3-Thiazolidine-2-thione

The monitored aminolysis of 3-acyl-1,3-thiazolidine-2-thiones has been extended to the peptide-bond formation, the chemoselective acylation of amino acids having multifunctional groups, and the crosslinking reaction between amino acids.

Synthesis and antibiotic efficiencies of di- and trialanyl derivatives of 6-aminopenicillanic and 7-aminocephalosporanic acid

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