67434-65-5

Usage

Uses

Used in Pharmaceutical Industry:
Pyrimidine, 4-chloro-5,6-dimethyl(7CI,9CI) is used as a building block for the synthesis of pharmaceutical drugs. Its unique structure and properties make it a valuable component in the development of new medications, contributing to the advancement of drug discovery and medicinal chemistry.
Used in Research Applications:
In the field of research, Pyrimidine, 4-chloro-5,6-dimethyl(7CI,9CI) is employed as a valuable tool for studying the properties and interactions of pyrimidine-based compounds. Its unique structure allows researchers to explore its potential applications in various chemical and biological processes.
Used in Chemical Manufacturing:
Pyrimidine, 4-chloro-5,6-dimethyl(7CI,9CI) is used as a precursor in the manufacturing of specialized chemicals and materials. Its unique chemical properties make it a key component in the production of various compounds and materials with specific characteristics and applications.

Upstream product

• 34916-78-4 5,6-dimethyl-3H-pyrimidin-4-one 
• 2302-39-8 4,5-dimethylimidazole 
• 67-66-3 chloroform 
• 609-14-3 2-acetylpropanoic acid ethyl ester 
• 28456-54-4 5,6-dimethyl-2-thiouracil 
• 34916-78-4 4-Hydroxy-5,6-dimethyl-pyrimidin 
• 4316-97-6 4,6-dichloro-5-methylpyrimidine 
• 13061-96-6 dihydroxy-methyl-borane 

Downstream Products

• 85073-88-7 (5,6-dimethyl-pyrimidin-4-yl)-phenyl-amine 
• 54568-12-6 4-Amino-5,6-dimethyl-pyrimidin 
• 85073-91-2 4-(4-Chloroanilino)-5,6-dimethylpyrimidine 
• 85074-13-1 4-(4-Isopropylanilino)-5,6-dimethylpyrimidine 

Relevant academic research and scientific papers

IMIDAZO [1, 2-C] PYRIMIDIN-2-YLMETHYLPIPERIDINES AS OREXIN RECEPTOR ANTAGONISTS

This invention relates to imidazo[1,2-c]pyrimidin-2-ylmethyl substituted piperidine derivatives and their use as pharmaceuticals.

PYRIMIDINE DERIVATIVES AND HERBICIDES CONTAINING THE SAME

The present invention provides a pyrimidine derivative represented by the formula: wherein R1p and R1q are the same or different, and each represents (1)hydrogen, (2)halogen, (3) a C1-6alkyl group which may be substituted or (4) a C1-6alkoxy group, and so on, R2 is halogen, a C1-6alkyl group, cyano group, and so on, Ar is a phenyl group which may be substituted or is a condensed hetero ring which may be substituted, which has excellent selective herbicidal activity, and a herbicide containing the derivative.

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.