133294-33-4

Basic information

• Product Name: Piperidine, 2-(2-propenyl)-, (S)- (9CI)
• Synonyms: Piperidine, 2-(2-propenyl)-, (S)- (9CI);(S)- 2-(2-PROPENYL)-PIPERIDINE;(2S)-2-PROP-2-ENYLPIPERIDINE
• CAS NO: 133294-33-4
• Molecular Formula: C8H15N
• Molecular Weight: 125.2114
• Product Categories: PIPERIDINE
• Mol File: 133294-33-4.mol
• Article Data: 13

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Piperidine, 2-(2-propenyl)-, (S)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Piperidine, 2-(2-propenyl)-, (S)- (9CI)(133294-33-4)
• EPA Substance Registry System: Piperidine, 2-(2-propenyl)-, (S)- (9CI)(133294-33-4)

Safety Data

• Hazardous Substances Data: 133294-33-4(Hazardous Substances Data)

Upstream product

• 20074-80-0 5-chloro-pentanal 
• 959420-89-4 (+)-(S)-N-[(1E)-5-chloropentylidene]-2-methylpropane-2-sulfinamide 
• 201350-80-3 (R)-tert-butyl 2-allylpiperidine-1-carboxylate 
• 184535-03-3 (S)-8-Azido-oct-1-en-4-ol 
• 184535-02-2 (S)-1-azido-5,6-epoxyhexane 
• 184535-01-1 (S)-6-azido-2-hydroxy-1-hexanol 
• 821-77-2 5-hexenylazide 
• 184535-04-4 Methanesulfonic acid (S)-1-allyl-5-azido-pentyl ester 
• 184535-14-6 (R)-8-Azido-oct-1-en-4-ol 
• 184535-13-5 (R)-1-azido-5,6-epoxyhexane 
• 184535-12-4 (R)-6-azidohexane-1,2-diol 
• 184535-15-7 Methanesulfonic acid (R)-1-allyl-5-azido-pentyl ester 
• 131248-69-6 1-[(E)-tert-Butylimino-methyl]-piperidin-2-one 
• 131248-73-2 2-methoxy piperidine N-t-butyl formamidine 

Downstream Products

• 1312812-27-3 (3R,4aS)-3-(chloromethyl)-2-(4-nitrophenyl)octahydro-1H-pyrido[1,2-c]pyrimidin-1-one 
• 1312812-31-9 (3aS,9aS,10aS)-3-(3,5-dichloro-2,4,6-trimethylphenyl)-3a,6,7,8,9,9a,10,10a-octahydroisoxazolo[5,4-b]quinolizin-4-one 
• 1312812-26-2 (3S,4aR)-3-(chloromethyl)-2-(4-nitrophenyl)octahydro-1H-pyrido[1,2-c]pyrimidin-1-one 
• 1312812-30-8 (3aR,9aR,10aR)-3-(3,5-dichloro-2,4,6-trimethylphenyl)-3a,6,7,8,9,9a,10,10a-octahydroisoxazolo[5,4-b]quinolizin-4-one 
• 705282-43-5 1-chloroformyl-2-(2-propenyl)piperidine 
• 491-40-7 quinolizidin-4-one 

Relevant articles and documents

Syntheses of nitrogen heterocycles by means of amine-directed carbonylation and hydrocarbonylation

Amine-directed carbonylation of 2-allylpiperidine (5) gives 8-methyl-1-azabicyclononan-9-one (7) with extremely high regio- and stereoselectivity, which is promoted by a stoichiometric amount of 2 in the presence of hydrogen chloride.A c

Stereocontrolled synthesis of bicyclic ureas and sulfamides via Pd-catalyzed alkene carboamination reactions

The synthesis of bicyclic ureas and sulfamides via palladium-catalyzed alkene carboamination reactions between aryl/alkenyl halides/triflates and alkenes bearing pendant cyclic sulfamides and ureas is described. The substrates for these reactions are gene

Enantiopure 2-piperidylacetaldehyde as a useful building block in the diversity-oriented synthesis of polycyclic piperidine derivatives

Novel, simple, and convenient strategies for diversely functionalized piperidine derivatives have been developed by using different metal catalyzed reactions starting from enantiopure (R)- and (S)-2-piperidylacetaldehyde.

Regioselective synthesis of azetidines or pyrrolidines by selenium-induced cyclization of secondary homoallylic amines

Azetidines or pyrrolidines can be regioselectively obtained by selenocyclization of homoallylic amines, according to the double bond substitution.