140445-85-8

Usage

Uses

Used in Organic Synthesis:
Pyridinium, 1-[chloro(4-methoxyphenyl)methyl]-, chloride is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions, contributing to the formation of desired products.
Used in Pharmaceutical Research:
In pharmaceutical research, Pyridinium, 1-[chloro(4-methoxyphenyl)methyl]-, chloride is used as a starting material or intermediate in the development of new drugs, leveraging its unique chemical structure and properties.
Used in Antimicrobial Applications:
Pyridinium, 1-[chloro(4-methoxyphenyl)methyl]-, chloride is used as an antimicrobial agent for its ability to inhibit the growth of microorganisms, making it suitable for applications in sanitization and preservation.
Used in Material Development:
Pyridinium, 1-[chloro(4-methoxyphenyl)methyl]-, chloride is also used in the research and development of new materials, where its chemical properties may contribute to the creation of innovative products with specific functionalities.
Used in Various Industries:
Pyridinium, 1-[chloro(4-methoxyphenyl)methyl]-, chloride finds applications across different industries, including but not limited to pharmaceuticals, agriculture, and chemical manufacturing, where its antimicrobial and synthetic properties are harnessed for diverse purposes.

Upstream product

• 110-86-1 pyridine 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 42972-34-9 diethyl 4-(4-methoxyphenyl)-1,2,6-trimethyl-1,4-dihydropyridine-3,5-dicarboxylate 
• 74979-66-1 1-Benzyl-4-(4-methoxy-phenyl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxylic acid diethyl ester 
• 34014-60-3 diethyl 1,4-dihydro-2,6-dimethyl-4-(4-methoxyphenyl)pyridine-3,5-dicarboxylate 
• 67205-04-3 2-(4-methoxyphenyl)quinazoline 
• 82408-02-4 3,3-dimethyl-2,3,4,5,10,11-hexahydro-11-[(4-methoxy)phenyl]-1H-dibenzo[b,e][1,4]diazepin-1-one 
• 67854-76-6 2-(4-Methoxy-phenyl)-1,2,3,4-tetrahydro-chinazolin 
• 74979-74-1 diethyl-1,4-bis(4-methoxyphenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate 

Relevant academic research and scientific papers

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

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 syntheses of heterocycles with N-(1-haloalkyl)azinium halides. Part 2. Preparation of N-unsubstituted 1,4-dihydropyridines

N-(1-Chloroalkyl)pyridinium chlorides, prepared from thionyl chloride, pyridine, and aldehydes, readily react with enaminocarbonyl derivatives to yield 1,4-dihydropyridines under mild and neutral conditions.

NOVEL SYNTHESES OF HETEROCYCLES WITH N-(1-HALOALKYL)AZINIUM HALIDES: PART 6. PREPARATION OF 2,3,4,5,10,11-HEXAHYDRO-1H-DIBENZODIAZEPIN-1-ONES

Conversion of aldehydes into N-(1-chloroalkyl)pyridinium chlorides (by means of pyridine and thionyl chloride) and further reaction with 3-(2-aminophenyl)amino-5,5-dimethyl-2-cyclohexenone provide a novel and efficient route to the title compounds.