223477-90-5

Basic information

• Product Name: 1-Piperidinecarboxylic acid, 2-(diphenylphosphinyl)-, 1,1-dimethylethyl ester
• CAS NO: 223477-90-5
• Molecular Formula: C22H28NO3P
• Molecular Weight: 385.443
• Mol File: 223477-90-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Piperidinecarboxylic acid, 2-(diphenylphosphinyl)-, 1,1-dimethylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Piperidinecarboxylic acid, 2-(diphenylphosphinyl)-, 1,1-dimethylethyl ester(223477-90-5)
• EPA Substance Registry System: 1-Piperidinecarboxylic acid, 2-(diphenylphosphinyl)-, 1,1-dimethylethyl ester(223477-90-5)

Safety Data

• Hazardous Substances Data: 223477-90-5(Hazardous Substances Data)

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 175857-65-5 2-(diphenylphosphinoyl)piperidine 
• 522-33-8 Tripiperidin 
• 4559-70-0 Diphenylphosphine oxide 

Downstream Products

• 302969-13-7 [2-(4-benzyloxy-benzo[1,3]dioxol-5-ylmethyl)-piperidin-1-yl]-(4-benzyloxy-3,5-dimethoxy-phenyl)-methanone 
• 302969-14-8 [2-(4-benzyloxy-benzo[1,3]dioxol-5-ylmethyl)-piperidin-1-yl]-(3,4,5-trimethoxy-phenyl)-methanone 
• 302969-12-6 2-(4-benzyloxy-benzo[1,3]dioxol-5-ylmethyl)-piperidine 
• 41447-09-0 (2RS)-1-[(2SR)-N-methylpiperidin-2-yl]propan-2-ol 
• 95018-41-0 2-benzyl-3,4,5,6-tetrahydropyridine 
• 847905-92-4 3-benzyl-4,6,7,8-tetrahydro-3H-pyrido[1,2-c][1,3]oxazin-1-one 
• 847905-88-8 tert-butyl (2E)-2-[(2E)-3-(4-methoxyphenyl)-2-propenylidene]piperidine-1-carboxylate 
• 302969-11-5 2-[1-(4-Benzyloxy-benzo[1,3]dioxol-5-yl)-meth-(E)-ylidene]-piperidine-1-carboxylic acid tert-butyl ester 

Relevant articles and documents

Synthesis of bicyclic carbamates as precursors of Sedum alkaloid derivatives

Synthesis of a N-Boc-protected piperidin-2-yl phosphine oxide starting from piperidine in three steps, followed by olefination using a variety of α,β-unsaturated aldehydes resulted in tert-butyl 2-(2′- alkenylidene)piperidine-1-carboxylates in high yields

Total syntheses of (±)-cryptopleurine, (±)-antofine and (±)- deoxypergularinine

The alkaloids (±)-cryptopleurine 1, (±)-antofine 2, and (±)- deoxypergularinine 3 were synthesized by Pictet-Spengler cyclization of the 2-arylmethylpiperidine and -pyrrolidines 4, 5 and 6 obtained by sequential N- deprotection-reduction of the parent ene