134557-58-7

Basic information

• Product Name: methyl-(+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate
• Synonyms: methyl-(+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate
• CAS NO: 134557-58-7
• Molecular Weight: 557.69
• Mol File: 134557-58-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl-(+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl-(+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate(134557-58-7)
• EPA Substance Registry System: methyl-(+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate(134557-58-7)

Safety Data

• Hazardous Substances Data: 134557-58-7(Hazardous Substances Data)

Upstream product

• 16108-03-5 n-formyl-tryptophan 
• 134558-12-6 methyl-(+/-)-β-<(phenylmethoxy)carbonyl>-β-<<(tricycl<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate 
• 135998-70-8 methyl-(+/-)-β-cyano-1-<(1,1-dimethylethoxy)carbonyl>-β-<(phenylmethoxy)carbonyl>-1H-indole 3-butanoate 
• 134558-13-7 methyl-(+/-)-β-carboxy-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate 
• 136019-52-8 benzyl-(+/-)-α-cyano-1-<(1,1-dimethylethoxy)carbonyl>-1H-indole-3-propanoate 
• 134558-10-4 1-<(1,1-dimethylethoxy)carbonyl>-N-formyl-DL-tryptophan benzyl ester 
• 134558-11-5 Methyl-(+/-)-β-amino-β[(phenylmethoxy)carbonyl]-1H-indole-3-butanoate 
• 134558-09-1 (+/-)-benzyl-N-formyltryptophan 
• 53120-53-9 2-adamantyl chloroformate 
• 64-04-0 phenethylamine 

Downstream Products

• 136019-53-9 tricyclo<3.3.1.1>dec-2-yl-(+/-)-<3-(1H-indol-3-ylmethyl)-2,5-dioxo-1-(2-phenylethyl)-3-pyrrolidinyl>carbamate 

Relevant articles and documents

Synthesis of an α-CH2CO2H functionalized tryptophan and its incorporation into an analogue of cholecystokinin

The synthesis of an α, α-bisubstituted tryptophan derivative (2) predicted by computer assisted molecular modelling to have close structural and conformational analogy to the endogenous neuropeptide cholecystokinin (CCK) is described. Central to the synth