96551-27-8

Basic information

• Product Name: α-methyl-(R)-tryptophan methyl ester
• Synonyms: α-methyl-(R)-tryptophan methyl ester
• CAS NO: 96551-27-8
• Molecular Weight: 232.282
• Mol File: 96551-27-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: α-methyl-(R)-tryptophan methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: α-methyl-(R)-tryptophan methyl ester(96551-27-8)
• EPA Substance Registry System: α-methyl-(R)-tryptophan methyl ester(96551-27-8)

Safety Data

• Hazardous Substances Data: 96551-27-8(Hazardous Substances Data)

Upstream product

• 96551-24-5 (3R,6S)-3-<<1-(tert-Butyloxycarbonyl)-3-indolyl>methyl>-3,6-dihydro-6-isopropyl-2,5-dimethoxy-3-methylpyrazin 
• 96551-23-4 (3R,6S)-3-1-(tert-Butyloxycarbonyl)-3,6-dihydro-2,5-dimethoxy-3,6-dimethylpyrazin 
• 96551-22-3 t-butyl 3-hydroxymethylindole-1-carboxylate 
• 96551-21-2 1-(t-butyloxycarbonyl)-3-(bromomethyl)indole 
• 487-89-8 Indole-3-carboxaldehyde 
• 96551-26-7 Methyl (R)-1-(tert-butyloxycarbonyl)-α-methyltryptophanate 
• 114524-80-0 methyl 2-(indol-3-ylmethyl)-2-aminopropionate 
• 57476-50-3 1-tert-butoxycarbonyl-3-formylindole 

Downstream Products

• 146929-49-9 -7-<<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-7-oxoheptanoic acid monohydrochloride 
• 146929-48-8 -6-<<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-6-oxohexanoic acid monohydrochloride 
• 146929-47-7 -5-<<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-5-oxopentanoic acid monohydrochloride 
• 146929-46-6 -4-<<2-<(2-amino-2-phenylethyl)amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-4-oxobutanoic acid monohydrochloride 
• 146953-14-2 methyl -7-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-7-oxoheptanoate 
• 146953-18-6 -7-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-7-oxoheptanoic acid 
• 148556-76-7 methyl -6-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-6-oxohexanoate 
• 146953-17-5 -6-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-6-oxohexanoic acid 
• 146953-12-0 ethyl -4-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-4-oxobutanoate 
• 146953-13-1 methyl -5-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-5-oxopentanoate 
• 146953-10-8 1,1-dimethylethyl -<2-<<3-(1H-indol-3-yl)-2-methyl-1-oxo-2-<<(phenylmethoxy)carbonyl>amino>propyl>amino>-1-phenylethyl>carbamate 
• 146953-16-4 -5-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-5-oxopentanoic acid 
• 146953-15-3 -4-<<2-<<2-<<(1,1-dimethylethoxy)carbonyl>amino>-2-phenylethyl>amino>-1-(1H-indol-3-ylmethyl)-1-methyl-2-oxoethyl>amino>-4-oxobutanoic acid 
• 146953-21-1 <2R-(2R*,6R*)>-2-(1H-indol-3-ylmethyl)-2-methyl-6-phenyl-1,4,7-triazacyclotridecan-3,8,13-trione 

Relevant articles and documents

Asymmetric Syntheses via Heterocyclic Intermediates, XXIV. - Enantioselective Synthesis of (R)-α-Methyltryptophane Methyl Ester and D-Tryptophane Methyl Ester by the Bislactim Ether Route

Die Titelverbindungen wurden durch asymmetrische Synthese nach der Bislactimether-Methode hergestellt (e.e. ueber 95percent bzw. etwa 90percent).