127896-76-8

Basic information

• Product Name: Pyridinium, 1-(chlorophenylmethyl)-, chloride
• CAS NO: 127896-76-8
• Molecular Formula: C12H11ClN.Cl
• Molecular Weight: 240.132
• Mol File: 127896-76-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Pyridinium, 1-(chlorophenylmethyl)-, chloride(CAS DataBase Reference)
• NIST Chemistry Reference: Pyridinium, 1-(chlorophenylmethyl)-, chloride(127896-76-8)
• EPA Substance Registry System: Pyridinium, 1-(chlorophenylmethyl)-, chloride(127896-76-8)

Safety Data

• Hazardous Substances Data: 127896-76-8(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 100-52-7 benzaldehyde 

Downstream Products

• 136397-25-6 5-benzylideneamino-4,5-dihydro-1,6-dimethyl-1H-pyrazolo<3,4-d>pyrimidin-4-one 
• 136397-28-9 5-benzylideneamino-3,4-dihydro-7-methyl-7H-pyrazolo<3,4-d>-1,2,3-triazi-4-one 
• 25855-20-3 2-phenylquinazoline 
• 37587-36-3 3,3-dimethyl-11-phenyl-2,3,4,5,10,11-hexahydro-1H-dibenzo<1,4>diazepin-1-one 
• 55661-71-7 2-phenyl-1,2,3, 4-tetrahydroquinazoline 
• 7182-99-2 4-benzylidenamino-benzoic acid ethyl ester 
• 5341-44-6 N-(3-nitrobenzylidene)aniline 
• 716-79-0 2-phenyl-1H-benzoimidazole 
• 717-57-7 N-benzylidene-o-phenylenediamine 
• 7519-65-5 N-(3-chlorobenzylidene)aniline 
• 1165-06-6 Diethyl 2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 67388-59-4 diethyl 1-(4-methoxyphenyl)-2,6-dimethyl-4-phenyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 56029-18-6 (Z)-2-Amino-3-{[1-phenyl-meth-(E)-ylidene]-amino}-but-2-enedinitrile 
• 66439-03-0 diethyl 1-benzyl-1,4-dihydro-2,6-dimethyl-4-phenylpyridine-3,5-dicarboxylate 

Relevant articles and documents

Synthesis of thiazolidine-4-carboxylic acids and N-(1-sulfonatoalkyl)pyridinium betaines from N-(1-chloroalkyl)pyrydinium chlorides

N-(1-chloroalkyl)pyridinium chlorides (1) react with L-cysteine to yield thiazolidine A-carboxylic acids.When salts 1 are not isolated, N-(1-sulfonatoalkyl)pyridinium betaines can be obtained under particular conditions.

A new and convenient method for the preparation of 2-substituted quinazolines

Aldehydes, converted in situ into N-(1-chloroalkyl)pyridinium chlorides using thionyl chloride and pyridine, react with 2-aminobenzylamine, under mild conditions, to yield 1,2,3,4-tetrahydroquinazolines. The latter can be aromatized readily by treatment w

Novel synthese of heterocycles with N-(1-haloalkyl)azinium halides. Part 5. Preparation of N-substituted 1,4-dihydropyridines

Thirty N-substituted Hantzsch 1,4-dihydropyridines were prepared under mild and neutral conditions from N-substituted enaminocarbonyl derivatives and aldehydes activated under the form of N-(1-chloroalkyl)pyridinium chlorides by means of thionyl chloride