59611-77-7

Basic information

• Product Name: 1-(chloro-phenyl-methylene)-piperidinium; chloride
• Synonyms: 1-(chloro-phenyl-methylene)-piperidinium; chloride
• CAS NO: 59611-77-7
• Molecular Weight: 244.164
• Mol File: 59611-77-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(chloro-phenyl-methylene)-piperidinium; chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(chloro-phenyl-methylene)-piperidinium; chloride(59611-77-7)
• EPA Substance Registry System: 1-(chloro-phenyl-methylene)-piperidinium; chloride(59611-77-7)

Safety Data

• Hazardous Substances Data: 59611-77-7(Hazardous Substances Data)

Upstream product

• 110-89-4 piperidine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 725-12-2 2,5-bis-(phenyl)-1,3,4-oxadiazole 
• 949-00-8 phenyl dithiobenzoate 
• 6295-81-4 N-benzylpiperidine hydrochloride 
• 936-63-0 S-ethyl dithiobenzoate 
• 95026-65-6 1-amino-2-(5-phenyl-[1,3,4]oxadiazol-2-yl)-anthraquinone 
• 1663-61-2 triethoxymethylbenzene 
• 936-61-8 Thiobenzoic acid O-ethyl ester 

Relevant articles and documents

Frustrated Lewis Pair Catalyzed Hydrogenation of Amides: Halides as Active Lewis Base in the Metal-Free Hydrogen Activation

A method for the metal-free reduction of carboxylic amides using oxalyl chloride as an activating agent and hydrogen as the final reductant is introduced. The reaction proceeds via the hydrogen splitting by B(2,6-F2-C6H3)3 in combination with chloride as the Lewis base. Density functional theory calculations support the unprecedented role of halides as active Lewis base components in the frustrated Lewis pair mediated hydrogen activation. The reaction displays broad substrate scope for tertiary benzoic acid amides and α-branched carboxamides.