140176-28-9

Basic information

• Product Name: 1-(carbobenzyloxy)-3-carbomethoxy-3-(phenylselenyl)-4-piperidone
• Synonyms: 1-(carbobenzyloxy)-3-carbomethoxy-3-(phenylselenyl)-4-piperidone
• CAS NO: 140176-28-9
• Molecular Weight: 446.361
• Mol File: 140176-28-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(carbobenzyloxy)-3-carbomethoxy-3-(phenylselenyl)-4-piperidone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(carbobenzyloxy)-3-carbomethoxy-3-(phenylselenyl)-4-piperidone(140176-28-9)
• EPA Substance Registry System: 1-(carbobenzyloxy)-3-carbomethoxy-3-(phenylselenyl)-4-piperidone(140176-28-9)

Safety Data

• Hazardous Substances Data: 140176-28-9(Hazardous Substances Data)

Upstream product

• 501-53-1 benzyl chloroformate 
• 71486-53-8 methyl 4-oxo-3-piperidinecarboxylate hydrochloride 
• 34837-55-3 Phenylselenyl bromide 
• 140176-27-8 1-oxo-1,3-piperidinedicarboxylic acid 1-benzyl ester 3-methyl ester 

Downstream Products

• 140176-49-4 1-(carbobenzyloxy)-2-<3,8,12,16-tetramethyl-3(E),7(E),11(E),15-heptadecatetraenyl>-4-piperidone 
• 140176-45-0 1-(carbobenzyloxy)-2-<4,8,12-trimethyl-3(E),7(E),11-tridecatrienyl>-4-piperidone 
• 140176-30-3 2-n-butyl-1,3-dimethyl-3-<<(p-toluenesulfonyl)oxy>methyl>-4-piperidone ethylene ketal 
• 135967-39-4 1-(carbobenzyloxy)-3-carbomethoxy-2-<3,8,12,16-tetramethyl-3(E),7(E),8(E),11(E),15-heptadecatrienyl>-4-piperidone 
• 135967-38-3 1-(carbobenzyloxy)-3-carbomethoxy-2-<4,8,12-trimethyl-3(E),7(E),11-tridecatrienyl>-4-piperidone 
• 135967-41-8 2-n-butyl-1-(carbobenzyloxy)-3-carbomethoxy-3-methyl-4-piperidone ethylene ketal 
• 135967-40-7 2-n-butyl-1-(carbobenzyloxy)-3-carbomethoxy-3-methyl-4-piperidone 
• 135967-35-0 2-n-butyl-1-(carbobenzyloxy)-3-carbomethoxy-4-piperidone 
• 135967-34-9 1-(carbobenzyloxy)-3-carbomethoxy-5,6-dihydro-4-pyridone 

Relevant articles and documents

Synthesis of Inhibitors of 2,3-Oxidosqualene-lanosterol Cyclase: Conjugate Addition of Organocuprates to N-(Carbobenzyloxy)-3-carbomethoxy-5,6-dihydro-4-pyridone

Synthesis of ammonium ion analogues of the first cationic intermediate, 5, presumed to be formed during the cyclization of 2,3-oxidosqualene by 2,3-oxidosqualene-lanosterol cyclase are reported.The required 2,3-substituted-4-piperidinols are prepared by c