682753-67-9

Basic information

• Product Name: L-Valine, N-[3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]-1H-indol-4-yl]-N-methyl-, phenylmethyl ester
• CAS NO: 682753-67-9
• Molecular Formula: C27H37BrN2O2Si
• Molecular Weight: 529.592
• Mol File: 682753-67-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: L-Valine, N-[3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]-1H-indol-4-yl]-N-methyl-, phenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: L-Valine, N-[3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]-1H-indol-4-yl]-N-methyl-, phenylmethyl ester(682753-67-9)
• EPA Substance Registry System: L-Valine, N-[3-bromo-1-[(1,1-dimethylethyl)dimethylsilyl]-1H-indol-4-yl]-N-methyl-, phenylmethyl ester(682753-67-9)

Safety Data

• Hazardous Substances Data: 682753-67-9(Hazardous Substances Data)

Upstream product

• 5192-23-4 4-amino-1H-indole 
• 682753-58-8 (S)-2-[1-(tert-butyl-dimethylsilyl)-1H-indol-4-ylamino]-3-methyl-butyric acid benzyl ester 
• 682753-54-4 (S)-2-(1H-indol-4-ylamino)-3-methyl-butyric acid benzyl ester 
• 78283-21-3 3-nitro-trans-2-[β-(dimethylamino)vinyl]-nitrobenzene 
• 606-20-2 2,6-dinitrotoluene 
• 682753-62-4 (S)-2-{[1-(tert-butyl-dimethylsilyl)-1H-indol-4-yl]-methylamino}-3-methyl-butyric acid benzyl ester 

Relevant articles and documents

A Regioselective Acylation of N-Substituted-4-Aminoindole. Its Application to the Synthesis of Indolactam V

Optically active (-) Indolactam V (1) was formally synthesized with the defined stereochemistry, through an efficient procedure via bromationlithiation in the 3-position of the indole ring using 2,6-dinitrotoluene and the aminoacids: D-serine and D-valine