7583-90-6

Basic information

• Product Name: 1-AMINO-2-METHYLPYRIDINIUM IODIDE
• Synonyms: 1-AMINO-2-METHYLPYRIDINIUM IODIDE;1-Amino-2-picolinium iodide;N-Amino-2-methylpyridinium iodide;N-Amino-2-picolinium iodide;2-methylpyridin-1-ium-1-amine iodide
• CAS NO: 7583-90-6
• Molecular Formula: C₆H₉N₂*I
• Molecular Weight: 236.05353
• Mol File: 7583-90-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 148-149℃
• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-AMINO-2-METHYLPYRIDINIUM IODIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-AMINO-2-METHYLPYRIDINIUM IODIDE(7583-90-6)
• EPA Substance Registry System: 1-AMINO-2-METHYLPYRIDINIUM IODIDE(7583-90-6)

Safety Data

• Hazardous Substances Data: 7583-90-6(Hazardous Substances Data)

Usage

General Description

1-AMINO-2-METHYLPYRIDINIUM IODIDE is a chemical compound with the molecular formula C6H9IN2. It is a salt that consists of a positively charged 1-amino-2-methylpyridinium ion and a negatively charged iodide ion. 1-AMINO-2-METHYLPYRIDINIUM IODIDE is commonly used in organic synthesis as a versatile reagent for various transformations, including the synthesis of pharmaceuticals, agrochemicals, and dyes. It is also used as a catalyst in certain chemical reactions. Additionally, 1-AMINO-2-METHYLPYRIDINIUM IODIDE has been studied for its potential applications in materials science, such as in the fabrication of organic-inorganic hybrid materials and as a component in ionic liquids. Overall, this compound has a wide range of uses in the field of chemistry and material science.

Upstream product

• 109-06-8 α-picoline 

Downstream Products

• 87290-07-1 C₁₃H₁₂N₂S 
• 100592-85-6 (7-Methyl-2-methylsulfanyl-pyrazolo[1,5-a]pyridin-3-yl)-phenyl-methanone 
• 28937-20-4 C₁₃H₁₃N₃S 
• 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 

Relevant articles and documents

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.

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