63812-16-8

Basic information

• Product Name: Piperidine, hydrofluoride
• CAS NO: 63812-16-8
• Molecular Formula: C5H11N.FH
• Molecular Weight: 105.155
• Mol File: 63812-16-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Piperidine, hydrofluoride(CAS DataBase Reference)
• NIST Chemistry Reference: Piperidine, hydrofluoride(63812-16-8)
• EPA Substance Registry System: Piperidine, hydrofluoride(63812-16-8)

Safety Data

• Hazardous Substances Data: 63812-16-8(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 6698-89-1 3,5-Cl₂C₆F₃SO₂F 
• 778-36-9 2,3,4,5,6-pentafluorobenzenesulfonamide 
• 120952-07-0 2-fluoro-N-ethylpyridinium tetraphenylborate 
• 20017-49-6 perfluoro-para-cymene 
• 319-82-4 decafluoro-m-xylene 
• 651-89-8 1,2,4,5-tetrafluoro-3,6-bis-trifluoromethyl-benzene 
• 1978-04-7 decafluoro-o-xylene 
• 434-64-0 perfluorotoluene 
• 793-92-0 1,3,5-trifluoro-2,4,6-tris(trifluoromethyl)benzene 
• 392-56-3 Hexafluorobenzene 

Relevant articles and documents

EFFECT OF THE NATURE OF THE LEAVING GROUP IN REACTIONS OF 2-X-N-ETHYLPYRIDINIUM SALTS WITH AMINES IN ACETONITRILE

The rate-determining stage in the nucleophilic substitution reactions of 2-X-N-ethylpyridinium salts with piperidine in acetonitrile changes, depending on the nature of the leaving group X.In the case where X = Hlg the controlling stage is the formation of the C-N bond.When X = 4-NO2C6H4O3, 3,4-(NO2)2C6H3O, and 2,6-(NO2)2C6H3O, nucleophilic substitution at the carbon atom is controlled by cleavage of the C-X bond.Nucleophilic substitution at a carbon atom of the benzene ring predominates in the reaction of 2-(2,4-dinitrophenoxy)-N-ethylpyridinium salt with piperidine.