944416-37-9

Basic information

• Product Name: (S)-2-amino-3-(3,4-dimethoxyphenyl)-N-methyl-propionamide
• Synonyms: (S)-2-amino-3-(3,4-dimethoxyphenyl)-N-methyl-propionamide
• CAS NO: 944416-37-9
• Molecular Weight: 238.287
• Mol File: 944416-37-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-2-amino-3-(3,4-dimethoxyphenyl)-N-methyl-propionamide(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-amino-3-(3,4-dimethoxyphenyl)-N-methyl-propionamide(944416-37-9)
• EPA Substance Registry System: (S)-2-amino-3-(3,4-dimethoxyphenyl)-N-methyl-propionamide(944416-37-9)

Safety Data

• Hazardous Substances Data: 944416-37-9(Hazardous Substances Data)

Upstream product

• 944416-22-2 [(S)-2-(3,4-dimethoxyphenyl)-1-methylcarbamoyl-ethyl]carbamic acid tert-butyl ester 
• 138908-56-2 (S)-(+)-2-tert-butoxycarbonylamino-3-(3,4-dimethoxyphenyl)propionic acid methyl ester 
• 111793-95-4 (3S,4R)-1-benzyl-3-<2-oxo-4(S)-phenyloxazolidinyl>-4-(3,4-dimethoxyphenyl)azetidin-2-one 
• 120346-33-0 (3S,4R)-1-methyl-3-<(4S)-phenyloxazolidinyl>-4-(3,4-dimethoxyphenyl)azetidin-2-one 
• 129077-93-6 (S)-(+)-3,4-dimethoxyphenylalanine ethyl ester hydrochloride 
• 74-89-5 methylamine 
• 32161-30-1 (S)-3,4-dimethoxyphenylalanine 
• 70494-48-3 (S)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-amine hydrochloride 
• 33859-00-6 benzyl-veratryliden-amine 
• 17972-14-4 N-(3,4-dimethoxybenzylidene)methanamine 

Downstream Products

• 944416-23-3 [(S)-1-((1R,3S)-6,7-dimethoxy-3-methylcarbamoyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethyl]carbamic acid benzyl ester 
• 944416-24-4 [(S)-1-((1S,3S)-6,7-dimethoxy-3-methylcarbamoyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethyl]carbamic acid benzyl ester 
• 944416-25-5 [(S)-1-((1R,3S)-6,7-dimethoxy-2-methyl-3-methylcarbamoyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethyl]carbamic acid benzyl ester 
• 944416-26-6 [(S)-1-((1S,3S)-6,7-dimethoxy-2-methyl-3-methylcarbamoyl-1,2,3,4-tetrahydroisoquinolin-1-yl)ethyl]carbamic acid benzyl ester 

Relevant articles and documents

Asymmetric and Geometry-Selective α-Alkenylation of α-Amino Acids

Both E- and Z-N′-alkenyl urea derivatives of imidazolidinones may be formed selectively from enantiopure α-amino acids. Generation of their enolate derivatives in the presence of K+ and [18]crown-6 induces intramolecular migration of the alkeny

Synthesis of tetrahydroisoquinoline-based pseudopeptides and their characterization as suitable reverse turn mimetics

New peptidomimetics containing the Tic moiety were synthesized in enantiomerically pure form and their conformational features were studied by NMR, IR, and molecular modeling techniques. The presence of a reverse turn conformation was observed in all the