4472-45-1

Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-2,6-dimethylpyrimidine is used as a key intermediate for the synthesis of various drugs, including antiviral and antifungal agents. Its unique structure allows for the development of new pharmaceutical compounds with enhanced therapeutic properties.
Used in Agrochemical Production:
4-CHLORO-2,6-DIMETHYLPYRIMIDINE serves as a building block in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals that protect crops and enhance yield.
Used in Dye Manufacturing:
4-Chloro-2,6-dimethylpyrimidine is utilized in the synthesis of dyes, providing a range of color options for various industries, including textiles, plastics, and printing.
Used in Fine Chemicals Industry:
As a versatile intermediate, 4-Chloro-2,6-dimethylpyrimidine is employed in the production of other fine chemicals, expanding its applications across different sectors.
Used in Organic Synthesis:
4-Chloro-2,6-dimethylpyrimidine acts as a precursor for the modification of other molecules, enabling the creation of new chemical compounds with diverse properties and applications in research and industry.

InChI:InChI=1/C6H7ClN2/c1-4-3-6(7)9-5(2)8-4/h3H,1-2H3

Upstream product

• 930-61-0 2,4-dimethyl-2-imidazoline 
• 67-66-3 chloroform 
• 930-62-1 2,4-Dimethylimidazole 

Downstream Products

• 86521-00-8 4-Ethynyl-2,6-dimethyl-pyrimidine 
• 77752-55-7 1,3'-dioxido-6'-(p-toluenesulfonyl)-2,2',6-trimethyl-4,4'-dipyrimidinylmethane 
• 77752-54-6 2,6-dimethyl-4-(p-toluenesulfonyl)pyrimidine 1-oxide 
• 77752-49-9 2,6-dimethyl-4-phenylsulfonylpyrimidine 
• 77752-58-0 2,6-dimethyl-4-(2-oxocyclohexyl)pyrimidine 
• 6622-92-0 2,6-dimethyl-1H-pyrimidin-4-one 
• 80602-01-3 dimethyloxosulfonium 2,6-dimethyl-4-pyrimidinyl-phenylcarbamoylmethylide 
• 80602-06-8 2-(2,6-Dimethyl-pyrimidin-4-yl)-N-phenyl-acetamide 
• 65845-63-8 2-(2,6-dimethyl-pyrimidin-4-yl)-1-phenyl-ethanone 
• 187875-70-3 1,5,7-trimethyl[1,2,4]triazolo[4,3-c]pyrimidinium-3-p-nitrophenylaminide 
• 187875-36-1 1-benzyl-1-(2,4-dimethylpyrimidin-6-yl)-4-ethoxycarbonylthisemicarbazide 
• 187875-12-3 1-methyl-1-(2,4-dimethylpyrimidin-6-yl)-4-p-nitrophenylthisemicarbazide 
• 187875-60-1 1,5,7-trimethyl[1,2,4]triazolo[4,3-c]pyrimidinium-3-p-tolylaminide 
• 187875-55-4 1,5,7-trimethyl[1,2,4]triazolo[4,3-c]pyrimidinium-3-phenylaminide 

Relevant academic research and scientific papers

Reactions of Halogenomethanes in the Vapor Phase. Part 4. The Reactions of Imidazoles with Chloroform at 550 deg C, and a Comparison with their Liquid-phase Reactions with Trichloroacetate Ion or Hexachloroacetone and Base

1-Unsubstituted imidazoles and chloroform at 550 deg C in a flow system give mainly 5-chloropyrimidines, together with 4-chloropyrimidines and chloropyrazines.The effects of methyl substituents on the ratio of products is considered.The liquid-phase reactions of 2-methyl- and 2,4,5-trimethyl-imidazole under conditions in which dichlorocarbene is said to be formed in basic or neutral conditions were studied, and compared with the gas-phase reactions with chloroform.

Reactions of Halogenomethanes in the Vapour Phase. Part 5. The Reactions of Imidazolines, Anils, and 1-Methylimidazole with Chloroform at 550 deg C, and a Comparison with their Liquid-Phase Reactions with Trichloroacetate Ion or Hexachloroacetone and Base

The vapor-phase reactions of imidazolines and anils with chloroform at 550 deg C are compared with their liquid-phase reactions in the presence of hexachloroacetone and base or upon thermolysis with trichloroacetate ion.In the vapour-phase reactions imidazolines, unlike imidazoles, gave non-chlorinated pyrimidines, and 1-methyl-imidazole gave 2-cyanopyrrole and the four 3-chlorocyanopyridines.