76970-14-4

Usage

Uses

Used in Pharmaceutical Industry:
3-Chloro-6-(3-methoxyphenyl)-pyridazine is used as an intermediate in the synthesis of pharmaceuticals for its potential applications in medicinal chemistry and drug development. Its unique structural features and reactivity allow for the creation of various biologically active molecules, contributing to the advancement of new therapeutic agents.
Used in Organic Compounds Synthesis:
In the field of organic chemistry, 3-chloro-6-(3-methoxyphenyl)-pyridazine is utilized as a key intermediate for the synthesis of a wide range of organic compounds. Its functional groups and reactivity make it a valuable component in the development of novel chemical entities with potential applications in various industries.

InChI:InChI=1/C11H9ClN2O/c1-15-9-4-2-3-8(7-9)10-5-6-11(12)14-13-10/h2-7H,1H3

Upstream product

• 95149-16-9 tris-(3-methoxy-phenyl)-bismuthane 
• 135034-10-5 3-chloro-6-iodopyridazine 
• 39499-65-5 4,5-dihydro-6-(3-methoxyphenyl)-3(2H)-pyridazinone 
• 76970-15-5 6-(3-methoxyphenyl)-2,3-dihydropyridazin-3-one 

Downstream Products

• 76970-03-1 6-(3-Methoxy-phenyl)-[1,2,4]triazolo[4,3-b]pyridazine 
• 76970-04-2 6-(3-Methoxy-phenyl)-3-methyl-[1,2,4]triazolo[4,3-b]pyridazine 

Relevant academic research and scientific papers

Pd-catalyzed chemoselective cross-coupling reaction of triaryl- or triheteroarylbismuth compounds with 3,6-dihalopyridazines

The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. The cross-coupling reactions of 3,6-dihalopyridazines with triaryl- or triheteroarylbismuth compounds were performed under palladium catalysis. The reaction was highly chemoselective, affording functionalized aryl- or heteroarylpyridazinyl chlorides in moderate to good yields. Copyright

Synthesis and Anxiolytic Activity of 6-(Substituted-phenyl)-1,2,4-triazolopyridazines

The synthesis of a series of 6-(substituted-phenyl)-1,2,4-triazolopyridazines (VIII) is reported.Some of these derivatives show activity in tests predictive of anxiolytic activity (a) protection against pentylenetetrazole-induced convulsions; (b)