886047-01-4

Basic information

• Product Name: 2-tert-butoxycarbonylamino-3-(2-phenylsulfanyl-1H-indol-3-yl)-propionic acid methyl ester
• Synonyms: 2-tert-butoxycarbonylamino-3-(2-phenylsulfanyl-1H-indol-3-yl)-propionic acid methyl ester
• CAS NO: 886047-01-4
• Molecular Weight: 426.536
• Mol File: 886047-01-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-tert-butoxycarbonylamino-3-(2-phenylsulfanyl-1H-indol-3-yl)-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-tert-butoxycarbonylamino-3-(2-phenylsulfanyl-1H-indol-3-yl)-propionic acid methyl ester(886047-01-4)
• EPA Substance Registry System: 2-tert-butoxycarbonylamino-3-(2-phenylsulfanyl-1H-indol-3-yl)-propionic acid methyl ester(886047-01-4)

Safety Data

• Hazardous Substances Data: 886047-01-4(Hazardous Substances Data)

Upstream product

• 13139-14-5 Boc-Trp-OH 
• 14204-24-1 N-(phenylthio)succinimide 
• 141215-69-2 methyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(1H-indol-3-yl)propanoate 
• 108-98-5 thiophenol 
• 931-59-9 benzenesulfenyl chloride 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 760968-18-1 2-tert-butoxycarbonylamino-3-(2-phenylsulfanyl-1H-indol-3-yl)-propionic acid 

Downstream Products

• 760967-97-3 C₂₂H₂₂N₂O₄S 
• 863976-61-8 methyl 3-(2-benzenesulfinyl-1H-indol-3-yl)-2-(tert-butoxycarbonyl)aminopropionate 

Relevant articles and documents

A conjugate Lewis base-Br?nsted acid catalyst for the sulfenylation of nitrogen containing heterocycles under mild conditions

Catalysts that contain a thiourea tethered to a carboxylic acid were found to affect the sulfenylation of indoles and other N-heterocycles on the hour time scale at room temperature. The mild nature of these conditions allowed for the incorporation of diverse functionalities into more complex heterocycles.