188562-93-8

Basic information

• Product Name: 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-en-yl trifluoromethanesulfonate
• Synonyms: 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-en-yl trifluoromethanesulfonate
• CAS NO: 188562-93-8
• Molecular Weight: 435.464
• Mol File: 188562-93-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-en-yl trifluoromethanesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-en-yl trifluoromethanesulfonate(188562-93-8)
• EPA Substance Registry System: 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-en-yl trifluoromethanesulfonate(188562-93-8)

Safety Data

• Hazardous Substances Data: 188562-93-8(Hazardous Substances Data)

Upstream product

• 145100-51-2 N-(5-chloropyridin-2-yl)-1,1,1-trifluoro-N-[(trifluoromethyl)sulphonyl]methanesulphonamide 
• 188562-91-6 tert-butyl N-benzyl(4-oxocyclohexyl)carbamate 
• 100-46-9 benzylamine 
• 142009-99-2 4-(benzylamino)cyclohexane-1-one 
• 131511-13-2 4-(N-benzylamino)cyclohexanone ethylene acetal 
• 4746-97-8 cyclohexanedione monoethylene ketal 

Downstream Products

• 188562-97-2 methyl 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-enecarboxylate 
• 188562-95-0 Benzyl-(4-cyano-cyclohex-3-enyl)-carbamic acid tert-butyl ester 
• 422507-09-3 4-[N-benzyl-N-(tert-butoxycarbonyl)amino]cyclohex-1-ene 
• 187807-24-5 4-{benzyl-[2-(methylselanyl)-2-oxoethyl]amino}cyclohex-1-ene 
• 422507-12-8 4-[N-benzyl-N-(methoxycarbonylmethyl)amino]-1-cyclohexene 
• 187807-23-4 N-benzyl-N-(3-cyclohexenyl)amine 

Relevant articles and documents

Synthesis of 2-azabicyclo[3.3.1]lnonanes by means of (carbamoyl)dichloromethyl radical cyclization

A new procedure for the synthesis of 2-azabicyclo[3.3.1]nonanes by intramolecular carboradical cyclization of 4-(trichloroacetamido)cyclohexenes substituted with an electron withdrawing substituent tester or nitrile) is described. The procedure allows the preparation of synthetically interesting azabicyclos 14 and 15 in nearly 70% yield.