135998-75-3

Basic information

• Product Name: benzyl-(+/-)-β-<<2-(trimethylsilyl)ethoxy>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-3-butanoate
• Synonyms: benzyl-(+/-)-β-<<2-(trimethylsilyl)ethoxy>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-3-butanoate
• CAS NO: 135998-75-3
• Molecular Weight: 630.857
• Mol File: 135998-75-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: benzyl-(+/-)-β-<<2-(trimethylsilyl)ethoxy>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-3-butanoate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl-(+/-)-β-<<2-(trimethylsilyl)ethoxy>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-3-butanoate(135998-75-3)
• EPA Substance Registry System: benzyl-(+/-)-β-<<2-(trimethylsilyl)ethoxy>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-3-butanoate(135998-75-3)

Safety Data

• Hazardous Substances Data: 135998-75-3(Hazardous Substances Data)

Upstream product

• 16108-03-5 n-formyl-tryptophan 
• 135998-74-2 phenylmethyl-(+/-)-β-cyano-1-<(1,1-dimethylethoxy)carbonyl>-β-<β-2-(trimethylsilyl)ethoxycarbonyl>-1H-indole-3-butanoate 
• 135998-73-1 2-(trimethylsilyl)ethyl-(+/-)-α-cyano-1-<(1,1-dimethylethoxy)carbonyl>-1H-indole-3-propanoate 
• 135998-72-0 1-<(1,1-dimethylethoxy)carbonyl>-N-formyl-DL-tryptophan-2-(trimethylsilyl)ethyl ester 
• 135998-71-9 (+/-)-2-(trimethylsilyl)ethyl-N-formyltryptophan 
• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 53120-53-9 2-adamantyl chloroformate 

Downstream Products

• 135998-76-4 benzyl-(+/-)-β-carboxyl-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate 
• 136019-51-7 (+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoic acid 
• 135998-77-5 benzyl-(+/-)-β-<<(2-phenylethyl)amino>carbonyl>-β-<<(tricyclo<3.3.1.1>dec-2-yloxy)carbonyl>amino>-1H-indole-3-butanoate 

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