38557-72-1

Usage

Uses

Used in Chemical Synthesis:
2-Chloro 3,5-dimethyl pyarazine is used as an intermediate in the chemical synthesis industry for the production of various compounds. Its unique structure allows it to serve as a building block for the creation of more complex molecules, which can be utilized in different fields such as pharmaceuticals, agrochemicals, and materials science.

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

Upstream product

• 1765-93-1 4-fluoroboronic acid 
• 930-62-1 2,4-Dimethylimidazole 
• 67-66-3 chloroform 
• 930-61-0 2,4-dimethyl-2-imidazoline 

Downstream Products

• 60187-00-0 3-hydroxy-2,6-dimethylpyrazine 
• 1092372-31-0 2-(4-fluorophenyl)-3,5-dimethylpyrazine 
• 1092372-30-9 2-(2,4-difluorophenyl)-3,5-dimethylpyrazine 
• 91678-81-8 2-amino-3,5-dimethyl pyrazine 
• 1383551-56-1 3,5-dimethyl-2-(3-diphenylaminophenyl)pyrazine 
• 1371537-32-4 3,5-dimethyl-2-(4-phenoxyphenyl)pyrazine 
• 1337916-22-9 3,5-imethyl-2-(7-phenylnaphthalen-2-yl)pyrazine 
• 1337916-16-1 3,5-dimethyl-2-(4-naphthalen-2-yl-phenyl)pyrazine 
• 1337916-14-9 3,5-dimethyl-2-(4-naphthalen-1-yl-phenyl)pyrazine 
• 1337916-19-4 3,5-dimethyl-2-(6-phenylnaphthalen-2-yl)pyrazine 
• 32350-16-6 3,5-dimethyl-2-propyl-pyrazine 
• 13925-07-0 2-ethyl-3,5-dimethylpyrazine 
• 33837-26-2 2-chloro-6-methoxy-5-methyl-3-phenyl-pyrazine 
• 92508-08-2 2-methoxy-3,5-dimethylpyrazine 

Relevant academic research and scientific papers

Organometallic Complex, and Light-Emitting Material, Light-Emitting Element, Light-Emitting Device and Electronic Device

The present invention provides a novel organometallic complex which emits green phosphorescence so as to enrich variations of phosphorescent materials for green color which is one of three primary colors. An organometallic complex comprising a structure represented by a general formula (G1) is provided. In the formula, R1 represents an alkyl group having 1 to 4 carbon atoms, and R2 and R3 individually represent hydrogen or an alkyl group having 1 to 4 carbon atoms. In addition, R4 to R7 individually represent an electron-withdrawing group, hydrogen or an alkyl group having 1 to 4 carbon atoms. Note that at least one of R4 to R7 represents an electron-withdrawing group. In addition, M is a central metal and represents either an element belonging to Group 9 in the periodic table or an element belonging to Group 10 in the periodic table.

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.