7583-90-6

Usage

Uses

Used in Organic Synthesis:
1-AMINO-2-METHYLPYRIDINIUM IODIDE is used as a reagent for various chemical transformations, facilitating the synthesis of pharmaceuticals, agrochemicals, and dyes. Its ability to participate in a range of reactions makes it a valuable tool in the development of new chemical entities.
Used as a Catalyst:
In certain chemical reactions, 1-AMINO-2-METHYLPYRIDINIUM IODIDE serves as a catalyst, enhancing the rate of these reactions without being consumed in the process. This role is crucial for improving the efficiency of industrial chemical processes.
Used in Materials Science:
1-AMINO-2-METHYLPYRIDINIUM IODIDE has been explored for its potential in the fabrication of organic-inorganic hybrid materials, contributing to the advancement of material properties and applications.
Used in Ionic Liquids:
As a component in ionic liquids, 1-AMINO-2-METHYLPYRIDINIUM IODIDE expands the scope of solvents and electrolytes, offering novel properties and applications in various chemical processes and technologies.
Overall, 1-AMINO-2-METHYLPYRIDINIUM IODIDE is a multifaceted compound with a broad spectrum of applications across the fields of chemistry and material science, underscoring its importance in both research and industrial applications.

Upstream product

• 109-06-8 α-picoline 

Downstream Products

• 87290-07-1 C₁₃H₁₂N₂S 
• 110911-74-5 C₁₇H₁₈ClN₂O₂S⁽¹⁺⁾*Br^(1-) 
• 110886-43-6 1-{[1-[2-(4-Chloro-phenyl)-2-oxo-ethylsulfanyl]-1-phenyl-meth-(Z)-ylidene]-amino}-2-methyl-pyridinium; bromide 
• 110886-65-2 1-{2-[2-(4-Chloro-phenyl)-2-oxo-ethyl]-3,3-dimethyl-isothioureido}-2-methyl-pyridinium; bromide 
• 110886-19-6 1-[1-[2-(4-Chloro-phenyl)-2-oxo-ethylsulfanyl]-prop-(Z)-ylideneamino]-2-methyl-pyridinium; bromide 
• 110886-40-3 2-Methyl-1-{[1-(2-oxo-2-phenyl-ethylsulfanyl)-1-phenyl-meth-(Z)-ylidene]-amino}-pyridinium; bromide 
• 110886-37-8 1-{[1-Ethoxycarbonylmethylsulfanyl-1-phenyl-meth-(Z)-ylidene]-amino}-2-methyl-pyridinium; bromide 
• 110886-86-7 C₁₇H₁₉N₂O₂S⁽¹⁺⁾*Br^(1-) 
• 110886-62-9 1-[3,3-Dimethyl-2-(2-oxo-2-phenyl-ethyl)-isothioureido]-2-methyl-pyridinium; bromide 
• 110886-34-5 1-{[1-Cyanomethylsulfanyl-1-phenyl-meth-(Z)-ylidene]-amino}-2-methyl-pyridinium; bromide 
• 110886-16-3 2-Methyl-1-[1-(2-oxo-2-phenyl-ethylsulfanyl)-prop-(Z)-ylideneamino]-pyridinium; bromide 
• 110911-98-3 C₁₅H₁₃ClN₂O₂S 
• 110911-95-0 C₁₅H₁₄N₂O₂S 
• 110886-48-1 7-Methyl-2-phenyl-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLO [1,5-α] PYRIDINE COMPOUNDS AND THEIR METHODS OF USE

The present invention is directed to substituted pyrazolo[l,5-α]pyridines and related methods for their synthesis and use.

Composition for the dyeing of keratin fibers comprising at least one 3-amino-pyrazolopyridine derivatives

Disclosed herein is a composition for the dyeing of keratin fibers, for example, human keratin fibers such as the hair, comprising at least one 3-amino pyrazolo-[1,5-a]-pyridine derivative or one of its addition salts and a method employing this derivative. The composition of the present disclosure makes it possible to obtain coloration in various shades that is powerful, chromatic, and aesthetic, with low selectivity and with good resistance to various aggressive factors to which the hair may be subjected, such as shampoos, the light, sweat and permanent shaping.

Non-imidazole heterocyclic histamine H3 receptor antagonists

Continued exploration of the SAR around the lead imidazopyridine histamine H3 antagonist 1 has led to the discovery of several related series of heterocyclic histamine H3 antagonists. The synthesis and SAR of indolizine, indole and p

2-Methylpyridinium Salts as 1,4-Dinucleophiles. IV. Westphal Condensation with 2-Alkyl-1-aminoazinium Substrates

Condensation of 2-alkyl-1-aminopyridinium, quinolinium or 1-alkyl-2-aminoisoquinolinium salts with 1,2-acenaphthenequinone or 9,10-phenanthrenequinone in the presence of base, gave pyridopyridazinium salts in good yields.