127478-20-0

Upstream product

• 289-80-5 1,2-diazine 
• 100-52-7 benzaldehyde 
• 53896-49-4 pyridazine-3-carbonitrile 
• 60905-93-3 3-benzyl-pyridazine 
• 63540-69-2 2-benzyl-2,5-dimethoxy-2,5-dihydro-furan 
• 37542-92-0 2-benzylfuran 
• 60906-52-7 phenyl (3-pyridazinyl) ketone 

Downstream Products

• 127494-99-9 3-α-chlorobenzylpyridazine 
• 60905-93-3 3-benzyl-pyridazine 
• 60906-52-7 phenyl (3-pyridazinyl) ketone 
• 136489-59-3 diphenyl(3-pyridazinyl)methanol 
• 136489-69-5 3-methoxy-6-(1-phenylethyl)pyridazine 
• 136489-66-2 1-phenyl-1-(3-pyridazinyl)ethanol 
• 136489-67-3 1-phenyl-1-(3-pyridazinyl)ethyl chloride 
• 136489-68-4 1-phenyl-1-(3-pyridazinyl)ethene 
• 127478-26-6 3-[(4-Methyl-piperazin-1-yl)-phenyl-methyl]-pyridazine 
• 127478-25-5 4-(Phenyl-pyridazin-3-yl-methyl)-morpholine 
• 127478-22-2 Methyl-phenyl-(phenyl-pyridazin-3-yl-methyl)-amine 
• 127478-28-8 Dimethyl-[2-(phenyl-pyridazin-3-yl-methylsulfanyl)-ethyl]-amine 
• 127478-24-4 3-(Phenyl-piperidin-1-yl-methyl)-pyridazine 
• 127478-27-7 3-(Phenyl-phenylsulfanyl-methyl)-pyridazine 

Relevant academic research and scientific papers

Diazines. 13. Metalation without Ortho-Directing Group Functionalization of Diazines via Direct Metalation

The successful metalation of diazines without an ortho-directing group is described.In some cases, dimers were obtained.The metalation was optimal with LTMP if a 4-fold excess of metalating agent was used, with a very short metalation reaction time at -75

Pyridazines. L . Syntheses and Reactions of Phenyl(3-pyridazinyl)methane Derivatives

A convenient approach to phenyl(3-pyridazinyl)ketone (6) and phenyl(3-pyridazinyl)methanol (7) is proposed.Reactions of the related diarylmethyl chloride 8 with various N- and S-nucleophiles were found to afford the expected amines 9a-c, 10a-c and thioeth

Pyridazine pesticides

Pyridazine derivatives of the formula: STR1 wherein R1 represents a fluorine, chlorine, bromine or iodine atom or an alkyl, alkoxy, alkylthio, alkylsulphonyl, nitro, trifluoromethyl, cyano, alkoxycarbonyl, carboxy, aminocarbonyl, amino, monoalkylamino or dialkylamino group, R2 represents a hydrogen atom or an alkyl group, R3 represents a hydrogen, fluorine, chlorine or bromine atom or an alkyl, methoxy, ethoxy or hydroxy group, or R2 and R3 together represent an oxygen atom or a hydroxyimino group, R4 represents a hydrogen atom or an alkyl group and n represents zero or an integer from 1 to 5 inclusive, are new compounds useful as herbicides.