79055-62-2

Basic information

• Product Name: 4-PYRIDINAMINE, 2-CHLORO-5-METHYL-
• Synonyms: 4-PYRIDINAMINE, 2-CHLORO-5-METHYL-;2-Chloro-5-Methyl-pyridin-4-ylaMine;4-aMino-2-chloro-5-Methylpyridine;2-Chloro-5-Methyl-4-pyridinaMine
• CAS NO: 79055-62-2
• Molecular Formula: C₆H₇ClN₂
• Molecular Weight: 142.588
• Mol File: 79055-62-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: 115℃
• Boiling Point: 283.3 °C at 760 mmHg
• Flash Point: 125.2 °C
• Appearance: /
• Density: 1.26 g/cm³
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 5.11±0.42(Predicted)
• CAS DataBase Reference: 4-PYRIDINAMINE, 2-CHLORO-5-METHYL-(CAS DataBase Reference)
• NIST Chemistry Reference: 4-PYRIDINAMINE, 2-CHLORO-5-METHYL-(79055-62-2)
• EPA Substance Registry System: 4-PYRIDINAMINE, 2-CHLORO-5-METHYL-(79055-62-2)

Safety Data

• Hazardous Substances Data: 79055-62-2(Hazardous Substances Data)

Usage

General Description

4-PYRIDINAMINE, 2-CHLORO-5-METHYL- is an organic compound with the molecular formula C6H6ClN3. It is a derivative of pyridine and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. This chemical is known to have both antimicrobial and herbicidal properties, making it useful in various applications. It is a white to off-white solid and should be handled with care due to its potential health hazards, including skin and eye irritation. Overall, 4-PYRIDINAMINE, 2-CHLORO-5-METHYL- has a range of industrial uses and is an important building block for the production of various compounds.

Upstream product

• 60323-96-8 2-chloro-5-methyl-4-nitropyridine 1-oxide 
• 97944-45-1 2-chloro-5-methyl-4-nitropyridine 
• 20173-49-3 2-chloro-5-methylpyridine-N-oxide 
• 18368-64-4 2-chloro-5-methylpyridine 

Downstream Products

• 787596-43-4 methyl 2-chloro-5-methylisonicotinate 
• 951030-56-1 2-chloro-5-methylisonicotinic acid 
• 1380324-13-9 C₂₂H₂₀ClF₂N₃O₄ 
• 1380324-14-0 2'-acetyl-3-chloro-4-[(2,4-difluorobenzyl)oxy]-5',6-dimethyl-2H-[1,4'-bipyridin]-2-one 
• 1380324-12-8 3-chloro-4-[(2,4-difluorobenzyl)oxy]-5',6-dimethyl-2-oxo-2H-[1,4'-bipyridine]-2'-carboxylic acid 
• 1380324-11-7 methyl 3-chloro-4-[(2,4-difluorobenzyl)oxy]-5',6-dimethyl-2-oxo-2H-[1,4'-bipyridine]-2'-carboxylate 
• 1380324-10-6 methyl 4-[(2,4-difluorobenzyl)oxy]-5',6-dimethyl-2-oxo-2H-1,4'-bipyridine-2'-carboxylate 
• 1380324-09-3 2'-chloro-4-[(2,4-difluorobenzyl)oxy]-5',6-dimethyl-2H-[1,4'-bipyridin]-2-one 
• 1380321-24-3 2'-[2-(tert-butyl)pyrimidin-4-yl]-3-chloro-4-((2,4-difluorobenzyl)oxy)-5',6-dimethyl-2H-[1,4'-bipyridin]-2-one 
• 1380321-23-2 3-chloro-4-((2,4-difluoropyridin-2-yl)methoxy)-2'-(2-(2-hydroxypropan-2-yl)pyrimidin-4-yl)-5',6-dimethyl-2H-[1,4'-bipyridin]-2-one 
• 1350646-91-1 7-(2-(2,5-difluorophenyl)-5-methylpyrimidin-4-ylamino)-N-ethyl-1H-pyrazolo[4,3-b]pyridine-1-carboxamide 
• 1350649-08-9 N-(2-(2,5-difluorophenyl)-5-methylpyrimidin-4-yl)-1-(4-methoxybenzyl)-1H-pyrazolo[4,3-b]pyridin-7-amine 
• 1350649-07-8 N-(2-(2,5-difluorophenyl)-5-methylpyrimidin-4-yl)-2-(4-methoxybenzyl)-2H-pyrazolo[4,3-b]pyridin-7-amine 

Relevant articles and documents

Selective sodium channel regulator, preparation and application thereof

The invention provides a compound as a selective sodium channel regulator, a synthesis method and a use method thereof, and particularly provides a compound as shown in a formula (I), a preparation method of the compound and application of the compound as the selective sodium channel regulator. The compounds exhibit excellent activity as sodium channel modulators.

2-hydroxy-4-amino-5-picoline heterocyclic compounds

The invention discloses a 2-hydroxy-4-amino-5-methylpyridine heterocyclic compound which can be used as an intermediate for synthesizing an omeprazole compound. The invention further discloses a synthesis method of a 2-hydroxy-4-amino-5-methylpyridine heterocyclic compound. The synthesis method comprises four steps of synthesis of 2-chloro-5-methylpyridine nitrogen oxide, synthesis of 2-chloro-4-nitro-5-methylpyridine nitrogen oxide, synthesis of 2-chloro-4-amino-5-methylpyridine and synthesis of 2-hydroxy-4-amino-5-methylpyridine. The synthesis method of the 2-hydroxy-4-amino-5-methylpyridine heterocyclic compound disclosed by the invention is simple, reaction raw materials are low in price, and a synthesis route is environment-friendly.

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