69025-13-4Relevant academic research and scientific papers
Synthesis and anticonvulsant activity of a new 6-alkoxy-[1,2,4]triazolo[4,3-b]pyridazine
Guan, Li-Ping,Sui, Xin,Deng, Xian-Qing,Quan, Ying-Chun,Quan, Zhe-Shan
scheme or table, p. 1746 - 1752 (2010/06/17)
A series of 6-alkoxy-[1,2,4]triazolo[4,3-b]pyridazine derivatives were synthesized. In initial screening and quantitative evaluation, compound 2r was among the most active agents, exhibiting in the same time the lowest toxicity. In the anti-maximal electr
Synthesis of some 3,6-disubstituted pyridazines
Shin, Mi-Seon,Kang, Young-Jin,Chung, Hyun-A.,Park, Jung-Won,Kweon, Deok-Heon,Lee, Woo Song,Yoon, Yong-Jin,Kim, Sung-Kyu
, p. 1135 - 1142 (2007/10/03)
Some novel 3-halo-6-(4-substituted-phenoxy)pyridazines and 3,6-di-(4- substituted-phenoxy)pyridazines were synthesized from 3,6-dichloropyridazine or 3,6-diiodopyridazine. 3,6-Diiodopyridazine was prepared from 3,6- dichloropyridazine using hydriodic acid/iodine monochloride.
Phenoxy pyridazinones and anorexigenic use thereof
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, (2008/06/13)
Compounds of the formula I STR1 in which R1 and R2 each represent a hydrogen atom, a halogen atom, an alkyl group containing 1 to 3 carbon atoms, an alkoxy group containing 1 to 3 carbon atoms or a trifluoromethyl group; and R3
