144630-67-1

Basic information

• Product Name: 2-(diphenylphosphoryl)pyrrolidine
• Synonyms: 2-(diphenylphosphoryl)pyrrolidine
• CAS NO: 144630-67-1
• Molecular Weight: 271.299
• Mol File: 144630-67-1.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(diphenylphosphoryl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(diphenylphosphoryl)pyrrolidine(144630-67-1)
• EPA Substance Registry System: 2-(diphenylphosphoryl)pyrrolidine(144630-67-1)

Safety Data

• Hazardous Substances Data: 144630-67-1(Hazardous Substances Data)

Upstream product

• 1499-21-4 Diphenylphosphinic chloride 
• 4559-70-0 Diphenylphosphine oxide 
• 5981-17-9 dodecahydro-3a,6a,9a-triaza-trindene 

Downstream Products

• 144630-68-2 5-<2-(diphenylphosphinyl)-2-methoxy-3-methyl-1-pyrrolidinyl>-1,4-benzoquinone 
• 184356-13-6 (3,4-Dimethoxy-phenyl)-[2-(diphenyl-phosphinoyl)-pyrrolidin-1-yl]-methanone 
• 223477-91-6 1-tert-butoxycarboxy-2-diphenylphosphinylpyrrolidine 
• 248253-35-2 [2-(diphenyl-phosphinoyl)-pyrrolidin-1-yl]-furan-2-yl-methanone 
• 248253-34-1 [2-(diphenyl-phosphinoyl)-pyrrolidin-1-yl]-(3,4,5-trimethoxy-phenyl)-methanone 
• 1099827-87-8 2-((R)-2-(diphenylphosphoryl)pyrrolidin-1-yl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol 
• 144630-69-3 1-<2,5-bis(benzyloxy)-4-methoxy-3-methylphenyl>-2-(diphenylphosphinyl)pyrrolidine 
• 302968-98-5 (4-benzyloxy-3,5-dimethoxy-phenyl)-[2-(diphenyl-phosphinoyl)-pyrrolidin-1-yl]-methanone 
• 206988-37-6 2-(Diphenyl-phosphinoyl)-pyrrolidine-1-carboxylic acid ethyl ester 
• 184356-14-7 [2-(Diphenyl-phosphinoyl)-pyrrolidin-1-yl]-p-tolyl-methanone 
• 94532-49-7 [2-(Diphenyl-phosphinoyl)-pyrrolidin-1-yl]-phenyl-methanone 

Relevant articles and documents

Reaction of N-(4,4-Diethoxybutyl)phosphamides with Chloro(diphenyl)phosphine. Synthesis of 2-(Diphenylphosphoryl)pyrrolidines

Abstract: The reaction of N-(4,4-diethoxybutyl)phosphamides with chloro(diphenyl)phosphine in chloroform in the presence of acetic acid gave previously unknown 2-(diphenylphosphoryl)pyrrolidines, and hydrolysis of the latter afforded 2-(diphenylphosphoryl

First synthesis and pharmacological evaluation of benzoindolizidine and benzoquinolizidine analogues of α- and β-peltatin

The benzoindolizidine and-quinolizidine analogues of α- and β-peltatin were designed and synthesized by two different synthetic routes involving as the key step the Bischler-Napieralski cyclization of suitably substituted N-acyl-2-arylmethylpyrrolidine and -piperidine derivatives. The in vitro biological activity of these analogues as well as some of their derivatives was subsequently evaluated. Copyright (C) 2000 Elsevier Science Ltd.

A new route to ene carbamates, precursors to benzoindolizinones through sequential asymmetric hydrogenation and cyclization

New pyrrolidine-based ene carbamates have been efficiently synthesized and the first example of asymmetric hydrogenation of this kind of substrate is reported, leading to the preparation of 2-arylmethylpyrrolidine precursors to benzoindolizinones in high