24049-46-5

Upstream product

• 1722-10-7 3-chloro-6-methoxypyridazine 
• 618-89-3 methyl 3-bromobenzoate 
• 1120-90-7 3-iodopyridine 
• 401-78-5 3-bromo-1-trifluoromethylbenzene 
• 392-83-6 o-trifluoromethylphenyl bromide 
• 2042-37-7 o-cyanobromobenzene 
• 610-94-6 2-bromobenzoic acid methyl ester 
• 2142-63-4 1-(3-Bromophenyl)ethanone 
• 78887-39-5 3-Acetamidophenylboronic acid 

Downstream Products

• 366-18-7 [2,2]bipyridinyl 

Relevant academic research and scientific papers

Preparation of functionalized aryl- and heteroarylpyridazines by nickel-catalyzed electrochemical cross-coupling reactions

(Chemical Equation Presented) A general efficient electrochemical method for the preparation of aryl- and heteroarylpyridazines in a nickel-catalyzed cross-coupling reaction of 3-chloro-6-methoxypyridazine and 3-chloro-6- methylpyridazine with a range of functionalized aryl or heteroaryl halides is reported.

Synthesis of substituted 3-amino-6-arylpyridazines via Suzuki reaction

Starting from the commercially available 3,6-dichloropyridazine, N3- substituted 3-amino-6-arylpyridazines were prepared in good yields and under mild conditions by means of two simple steps: a nucleophilic substitution and a palladium-catalyzed Suzuki coupling.