207554-43-6

Basic information

• Product Name: S-(2-((tert-butoxycarbonyl)amino)ethyl) benzothioate
• Synonyms: S-(2-((tert-butoxycarbonyl)amino)ethyl) benzothioate
• CAS NO: 207554-43-6
• Molecular Weight: 281.376
• Mol File: 207554-43-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: S-(2-((tert-butoxycarbonyl)amino)ethyl) benzothioate(CAS DataBase Reference)
• NIST Chemistry Reference: S-(2-((tert-butoxycarbonyl)amino)ethyl) benzothioate(207554-43-6)
• EPA Substance Registry System: S-(2-((tert-butoxycarbonyl)amino)ethyl) benzothioate(207554-43-6)

Safety Data

• Hazardous Substances Data: 207554-43-6(Hazardous Substances Data)

Upstream product

• 6343-27-7 1-benzoylpyrrolidine-2,5-dione 
• 67385-09-5 2-[(tert-butoxycarbonyl)amino]-1-ethanethiol 
• 538-86-3 benzyl methyl ether 
• 39684-80-5 2-(tert-butoxycarbonylamino)ethyl bromide 
• 98-88-4 benzoyl chloride 
• 10489-23-3 S-1-octyl benzothioate 
• 67385-10-8 di-tert-butyl(disulfanediylbis(ethane-2,1-diyl))dicarbamate 
• 4530-20-5 BOC-glycine 
• 98-91-9 thiobenzoic acid 
• 26690-80-2 2-(N-tert-butoxycarbonylamino)ethanol 

Downstream Products

• 17612-90-7 S-benzoylcysteamine hydrochloride 

Relevant articles and documents

Metal-free thioesterification of amides generating acyl thioesters

A base-initiated thioesterification of amides with various thiols is reported. This reaction can take place efficiently under metal-free and air-atmospheric conditions, and provides a facile and practically useful approach to the synthesis of valuable acy

An odorless, one-pot synthesis of thioesters from organic halides, thiourea and benzoyl chlorides in water

Thioesterification can be realized via an odorless, one-pot reaction through the in situ generation of S-alkylisothiouronium salts from organic halides and thiourea in aqueous Triton X-100 (TX100) micelles. The protocol is free of foul-smell thiols and or

"Inverse" type of synthetic inhibitors of trypsin, S-omega-aminoalkyl thioesters.

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