741633-48-7

Basic information

• Product Name: 2-Piperidinecarbonyl chloride, (S)- (9CI)
• Synonyms: 2-Piperidinecarbonyl chloride, (S)- (9CI)
• CAS NO: 741633-48-7
• Molecular Formula: C₆H₁₀ClNO
• Molecular Weight: 147.6027
• Product Categories: ACIDHALIDE
• Mol File: 741633-48-7.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Piperidinecarbonyl chloride, (S)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Piperidinecarbonyl chloride, (S)- (9CI)(741633-48-7)
• EPA Substance Registry System: 2-Piperidinecarbonyl chloride, (S)- (9CI)(741633-48-7)

Safety Data

• Hazardous Substances Data: 741633-48-7(Hazardous Substances Data)

Upstream product

• 136598-30-6 (S)-1-(ethoxycarbonyl)pipecolic acid 
• 3105-95-1 pipecolinic acid 

Downstream Products

• 1192124-69-8 (S)-Piperidin-2-yl-piperidin-1-yl-methanone 
• 130497-29-9 (S)-Piperidine-2-carboxylic acid dimethylamide 
• 130497-30-2 (S)-N,N-diethylpiperidine-2-carboxamide 
• 120990-93-4 Diethyl-(S)-1-piperidin-2-ylmethyl-amine 
• 130497-15-3 2-(3,4-Dichloro-phenyl)-1-((S)-2-diethylaminomethyl-piperidin-1-yl)-ethanone 
• 112419-07-5 Dimethyl-(S)-1-piperidin-2-ylmethyl-amine 
• 130497-37-9 2-(3,4-Dichloro-phenyl)-1-((S)-2-dimethylaminomethyl-piperidin-1-yl)-ethanone 
• 130497-47-1 2-(4-tert-Butyl-phenyl)-1-((S)-2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone 
• 130497-34-6 BRL 52537 
• 130497-40-4 (2S)-1-[[4-trifluoromethyl-phenyl]acetyl]-2-[(1-pyrrolidinyl)methyl]piperidine 
• 19889-77-1 (2S)-2-piperidinecarboxamide 
• 19889-77-1 (+)-2R-Piperidine-2-carboxylic acid amide 
• 251916-58-2 (S)-1-(benzylsulfonyl)piperidine-2-carboxylic acid 

Relevant articles and documents

Stereoselective synthesis of (?)-3-PPP through palladium-catalysed unactivated C(sp3)–H arylation at the C-3 position of L-pipecolinic acid

An efficient route for the preparation of (?)-3-PPP(preclamol) using the highly stereoselective palladium-catalysed C(sp3)-H arylation and radical decarboxylation reaction as the key steps is described. The chiral center at the C-3 position of

The synthesis and conformational analysis of optical isomers of 4-phenyl-perhydropyrido[1,2-a]pyrazine-1,3-dione: an example of 'solid state-frozen' dynamics in nitrogen-bridged bicyclic 2,6-diketopiperazines

The synthesis, chemical properties, and conformational analysis of enantiopure (4R,9aS)-, (4S,9aR)-, (4S,9aS)-, and (4R,9aR)-4-phenyl-perhydropyrido[1,2-a]pyrazine-1,3-diones having potential biological activity are described. An interesting example of the coexistence of two invertomers of the (4R,9aR)-diastereomer in a single crystal unit cell is reported. The invertomers differ in the cis/trans-relationship between the fused rings and in the absolute configuration at the chiral nitrogen atom. The structure and equilibrium distributions of the respective conformers have been determined by NMR spectroscopy in both polar and non-polar solvents at various temperatures. The NMR spectra show that dynamic processes in the imide parts of the interconverting species are restrained by self-aggregation. The (4S,9aR)-diastereomer exists in a single conformation with insignificant dynamic effects.