28945-11-1

Basic information

• Product Name: L-Alanine, N-acetyl-L-phenylalanyl-, methyl ester
• CAS NO: 28945-11-1
• Molecular Formula: C15H20N2O4
• Molecular Weight: 292.335
• Mol File: 28945-11-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: L-Alanine, N-acetyl-L-phenylalanyl-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Alanine, N-acetyl-L-phenylalanyl-, methyl ester(28945-11-1)
• EPA Substance Registry System: L-Alanine, N-acetyl-L-phenylalanyl-, methyl ester(28945-11-1)

Safety Data

• Hazardous Substances Data: 28945-11-1(Hazardous Substances Data)

Upstream product

• 42291-21-4 AcΔPheAlaOH 
• 76741-27-0 (3S,4R,1'S)-1-(1'-Methoxycarbonyl)ethyl-3-azido-4-phenylazetidin-2-one 
• 53933-42-9 2-(benzylidene-amino)-propionic acid methyl ester 
• 55065-02-6 N-acetamido cinnamic acid 
• 65941-25-5 Ac-ΔPhe-(S)-Ala-OH 
• 2018-61-3 (S)-2-acetylamino-3-phenylpropanoic acid 
• 2491-20-5 L-alanine methyl ester hydrochloride 
• 543-27-1 isobutyl chloroformate 
• 10065-72-2 L-Alanine methyl ester 
• 108395-58-0 acetyl L-phenylalanine chloroethyl ester 
• 74986-31-5 AcΔPhe(RS)AlaOMe 
• 76741-29-2 (S)-2-((3S,4R)-3-Acetylamino-2-oxo-4-phenyl-azetidin-1-yl)-propionic acid methyl ester 
• 94943-62-1 Ac-Δ-Ph-(S)-Ala-OCH3 
• 67-56-1 methanol 

Relevant articles and documents

Stereoselective Synthesis of Dipeptides by Asymmetric Reduction of Dehydropeptides Catalyzed by Chiral Rhodium Complexes

Asymmetric catalysis was used to control the creation of an asymmetric center in a chiral dehydropeptide.The reduction of Ac-ΔPhe-(S)-Phe-OR (R=H or Me) was studied as a model.Depending on the type of chiral rhodium catalyst used, it was possible to selec

Chiral sulfonated phosphines. VIII. Hydrogenation of dehydropeptides in a two-phase system

Dehydropeptides have been reduced in a two-phase system using 2> associated with chiral water-soluble ligands derived from cyclobutanediop and BDPP.Diastereoselectivities of up to 87percent were obtained with tetrasulfonated BDPP.

Effects of solvent and temperature on the 1,4-asymmetric induction in the diastereoselective hydrogenation of dehydrodipeptides

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