1588517-15-0

Basic information

• Product Name: tert-butyl 3-(2-((tert-butoxycarbonyl)amino)-2-(4-cyanophenyl)ethyl)-1H-indole-1-carboxylate
• Synonyms: tert-butyl 3-(2-((tert-butoxycarbonyl)amino)-2-(4-cyanophenyl)ethyl)-1H-indole-1-carboxylate
• CAS NO: 1588517-15-0
• Molecular Weight: 461.561
• Mol File: 1588517-15-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: tert-butyl 3-(2-((tert-butoxycarbonyl)amino)-2-(4-cyanophenyl)ethyl)-1H-indole-1-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl 3-(2-((tert-butoxycarbonyl)amino)-2-(4-cyanophenyl)ethyl)-1H-indole-1-carboxylate(1588517-15-0)
• EPA Substance Registry System: tert-butyl 3-(2-((tert-butoxycarbonyl)amino)-2-(4-cyanophenyl)ethyl)-1H-indole-1-carboxylate(1588517-15-0)

Safety Data

• Hazardous Substances Data: 1588517-15-0(Hazardous Substances Data)

Upstream product

• 144599-95-1 N^α-(tert-butoxycarbonyl)-1-methyl-L-tryptophan 
• 623-26-7 terephthalonitrile 

Relevant articles and documents

Decarboxylative arylation of α-Amino acids via photoredox catalysis: A one-step conversion of biomass to drug pharmacophore

The direct decarboxylative arylation of α-amino acids has been achieved via visible light-mediated photoredox catalysis. This method offers rapid entry to prevalent benzylic amine architectures from an abundant biomass, specifically α-amino acid precursors. Significant substrate scope is observed with respect to both the amino acid and arene components.