367924-67-2

Basic information

• Product Name: benzyl {(S)-1-{{{-2-{{(R)-1-benzyl-1-methyl-2-{methyl[(R)-1-(naphthalen-1-yl)ethyl]amino}-2-oxoethyl}amino}-1,1-dimethyl-2-oxoethyl}amino}oxomethyl}-3-methylbutyl}carbamate
• Synonyms: benzyl {(S)-1-{{{-2-{{(R)-1-benzyl-1-methyl-2-{methyl[(R)-1-(naphthalen-1-yl)ethyl]amino}-2-oxoethyl}amino}-1,1-dimethyl-2-oxoethyl}amino}oxomethyl}-3-methylbutyl}carbamate
• CAS NO: 367924-67-2
• Molecular Weight: 678.872
• Mol File: 367924-67-2.mol

Chemical Properties

• CAS DataBase Reference: benzyl {(S)-1-{{{-2-{{(R)-1-benzyl-1-methyl-2-{methyl[(R)-1-(naphthalen-1-yl)ethyl]amino}-2-oxoethyl}amino}-1,1-dimethyl-2-oxoethyl}amino}oxomethyl}-3-methylbutyl}carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl {(S)-1-{{{-2-{{(R)-1-benzyl-1-methyl-2-{methyl[(R)-1-(naphthalen-1-yl)ethyl]amino}-2-oxoethyl}amino}-1,1-dimethyl-2-oxoethyl}amino}oxomethyl}-3-methylbutyl}carbamate(367924-67-2)
• EPA Substance Registry System: benzyl {(S)-1-{{{-2-{{(R)-1-benzyl-1-methyl-2-{methyl[(R)-1-(naphthalen-1-yl)ethyl]amino}-2-oxoethyl}amino}-1,1-dimethyl-2-oxoethyl}amino}oxomethyl}-3-methylbutyl}carbamate(367924-67-2)

Safety Data

• Hazardous Substances Data: 367924-67-2(Hazardous Substances Data)

Upstream product

• 367924-10-5 N-methyl-N-[(R)-1-(naphthalen-1-yl)ethyl]propanamide 
• 116837-58-2 N-[(R)-1-(naphthalen-1-yl)ethyl]propanamide 
• 3886-70-2 (R)-1-(1-Naphthyl)ethylamine 
• 2018-66-8 Z-Leu-OH 
• 128422-11-7 N-[(benzyloxy)carbonyl]leucyl-α-aminoisobutyric acid 
• 367924-40-1 (R)-2-benzyl-2,N-dimethyl-N-[(R)-1-(naphthalen-1-yl)ethyl]-2H-azirin-3-amine 

Downstream Products

• 1029991-81-8 (R)-2-benzyl-2-({2-[((S)-2-{[(benzyloxy)carbonyl]amino}-4-methyl-1-oxopentyl)amino]-2-methyl-1-oxopropyl}amino)propanoic acid 

Relevant articles and documents

New optically active 2H-azirin-3-amines as synthons for enantiomerically pure 2,2-disubstituted glycines

The synthesis of novel 2,2-disubstituted 2H-azirin-3-amines with a chiral amino group is described. Chromatographic separation of the diastereoisomer mixture yielded the pure diastereoisomers (1′R,2R)-4a-e and (1′R,2S)-4a-e (Scheme 1, Table 1), which are