2096-22-2

Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-4,5-dimethoxypyridazine is used as a building block in organic synthesis for the development of new pharmaceutical compounds. Its unique structure and biological activities make it a promising candidate for the creation of novel drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Chloro-4,5-dimethoxypyridazine serves as a precursor in the production of various agrochemicals. Its potential use in this industry highlights its versatility and the possibility of contributing to the development of innovative solutions for agricultural challenges.
Used as a Research Tool:
3-Chloro-4,5-dimethoxypyridazine is also utilized as a research tool in chemical and biological studies. Its unique properties and potential applications make it valuable for exploring new scientific frontiers and advancing our understanding of various chemical and biological processes.

Upstream product

• 124-41-4 sodium methylate 
• 2288-74-6 3,5-dichloro-4-methoxypyridazine 
• 63910-32-7 3,4-dichloro-5-methoxy-pyridazine 

Downstream Products

• 1357358-22-5 1-cyclobutyl-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 
• 1357358-03-2 5-methoxy-1-methyl-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 
• 1357192-29-0 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-pyridin-2-ylpyridazin-4(1H)-one 
• 1357192-36-9 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-pyrimidin-5-ylpyridazin-4(1H)-one 
• 55271-48-2 4,5-dimethoxy-pyridazine 
• 1357358-24-7 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-(2,2,2-trifluoroethyl)pyridazin-4(1H)-one 
• 1357592-87-0 1-cyclopropyl-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 
• 1357591-80-0 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-[2-(trifluoromethyl)benzyl]pyridazin-4(1H)-one 
• 1357591-77-5 1-[1-(diphenylmethyl)azetidin-3-yl]-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 
• 1357590-85-2 1-(biphenyl-3-ylmethyl)-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 
• 1357590-79-4 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-(phenylsulfonyl)pyridazin-4(1H)-one 
• 1357358-05-4 1-(cyclopropylmethyl)-5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one 
• 1357590-67-0 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)-1-(1,2,3,4-tetrahydronaphthalen-2-yl)pyridazin-4(1H)-one 
• 1357192-32-5 5-methoxy-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4-ol 

Relevant academic research and scientific papers

TRIAZOLE-PYRIDINYL SUBSTITUTED AZACYCLOHEXYL ACETIC ACID COMPOUNDS AS LPA RECEPTOR ANTAGONISTS

This application relates to novel substituted azacyclohexyl acetic acid compounds, their manufacture, pharmaceutical compositions comprising them, and their use as medicaments for treating a disease associated with dysregulation of lysophosphatidic acid receptors (LPA).

Studies on Syntheses and Reaction of Methoxypyridazines. I. Methoxylation of 3,4,5-Trichloropyridazine

The reaction of 3,4,5-trichloropyridazine (1) with 1 eq amount of NaOMe resulted in the formation of three dichloromonomethoxypyridazines (2, 3-OMe; 3, 4-OMe; 4, 5-OMe) in the ratio of 1:3:6.The 4-OMe compound 3 was isolated from the reaction mixture and the 3-OMe compound 2 was syntesizsed independently.Further methoxylation of 2, 3 and 4 was also investigated in order to prepare various substituted pyrazines.Keywords - 3,4,5-trichloropyridazine; methoxylation; dichloromonomethoxypyridazine; monochlorodimethoxypyridazine; pyridazinone; 3,4,5-trimethoxypyridazine