1780-36-5

Usage

Uses

Used in Pharmaceutical Industry:
2,4,6-Trichloro-5-methylpyrimidine is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the creation of new drugs, potentially leading to advancements in the treatment of various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,6-Trichloro-5-methylpyrimidine serves as an intermediate in the production of agrochemicals. Its incorporation into these products can enhance crop protection and contribute to the development of more effective pesticides.
Safety Considerations:

InChI:InChI=1/C6H13NO/c7-5-2-1-3-6(8)4-5/h5-6,8H,1-4,7H2

Upstream product

• 10025-87-3 trichlorophosphate 
• 2417-22-3 5-methylbarbituric acid 
• 2565-47-1 1-methyl-2,4,6-pyrimidinetrione 

Downstream Products

• 2036-41-1 5-methylpyrimidine 
• 22536-61-4 2-chloro-5-methylpyrimidine 
• 71735-34-7 5-methyl-2,4,6-triaminopyrimidine 
• 1780-37-6 5-Brommethyl-2,4,6-trichlor-pyrimidin 
• 22433-68-7 4-Amino-5-methylpyrimidin 
• 18588-37-9 5-methylpyrimidine-2,4-diamine 
• 162706-07-2 5-methyl-pyrimidine-4,6-diyldiamine 
• 1627-28-7 6-chloro-5-methylpyrimidine-2,4(1H,3H)-dione 
• 31458-38-5 6-iodo-5-methylpyrimidine-2,4(1H,3H)-dione 

Relevant academic research and scientific papers

Polyazidopyrimidines: High-energy compounds and precursors to carbon nanotubes

(Figure Presented) An additional azidomethyl group dramatically decreases the melting points of the corresponding azidopyrimidines. Theoretical calculations show that these polyazido compounds (see picture; N light blue, C dark blue, H white) exhibit high

Method for synthesizing 2,4,6,-trichlorine-5-methyl pyridine

The invention discloses a method for synthesizing 2,4,6,-trichlorine-5-methyl pyridine. The method for synthesizing the 2,4,6,-trichlorine-5-methyl pyridine comprises the steps that after the 2,4,6,-trichlorine-5-methyl pyridine, phosphorus oxychloride an

IMAGING AGENTS

The present invention relates to radiolabelled 4-(furo[3,2-c]pyridin-4-yl) derivatives and their use as radioactive tracers, and in particular their use as imaging agents.

Functionalization of unprotected uracil derivatives using the halogen - Magnesium exchange

The reaction of commercially available 5-iodouracil with 2 equiv of MeMgCl in the presence of LiCl, followed by the addition of i-PrMgCl-LiCl, provides the corresponding trimagnesiated species, which reacts with various electrophiles to give selectively 5

Pyrimidine derivatives having a herbicidal action and an action regulating plant growth

N-Pyrimidin-4-yl-N'-sulfonylureas of the formula I and the basic addition salts thereof have herbicidal properties and properties for regulating, especially inhibiting, plant growth: STR1 the symbols in this formula having the following meanings: Q is hal