60905-93-3

Upstream product

• 1632-76-4 3-methylpyridazine 
• 108-86-1 bromobenzene 
• 63540-69-2 2-benzyl-2,5-dimethoxy-2,5-dihydro-furan 
• 37542-92-0 2-benzylfuran 
• 91344-47-7 2-Furfuryl-phenol 
• 73535-73-6 2‐(6‐chloropyridazin‐3‐yl)‐2‐phenylacetonitrile 
• 140-29-4 phenylacetonitrile 
• 90230-87-8 3-Benzylpyridazine 2-oxide 
• 127478-20-0 phenyl(3-pyridazinyl)methanol 

Downstream Products

• 90230-87-8 3-Benzylpyridazine 2-oxide 
• 90210-58-5 3-Benzylpyridazine 1-oxide 
• 60906-52-7 phenyl (3-pyridazinyl) ketone 
• 127494-99-9 3-α-chlorobenzylpyridazine 
• 127478-20-0 phenyl(3-pyridazinyl)methanol 
• 127478-23-3 3-(Phenyl-pyrrolidin-1-yl-methyl)-pyridazine 
• 127478-27-7 3-(Phenyl-phenylsulfanyl-methyl)-pyridazine 
• 127478-24-4 3-(Phenyl-piperidin-1-yl-methyl)-pyridazine 
• 127478-28-8 Dimethyl-[2-(phenyl-pyridazin-3-yl-methylsulfanyl)-ethyl]-amine 
• 127478-22-2 Methyl-phenyl-(phenyl-pyridazin-3-yl-methyl)-amine 
• 127478-25-5 4-(Phenyl-pyridazin-3-yl-methyl)-morpholine 
• 127478-26-6 3-[(4-Methyl-piperazin-1-yl)-phenyl-methyl]-pyridazine 

Relevant academic research and scientific papers

Telesubstitution and Dismutation Reactions in the Series of Phenyl-3-pyridazinylmethane Derivatives

Reactions of 3-α-chlorobenzylpyridazine (4) with alkoxides have been found to yield 6-substituted or 4-substituted 3-benzylpyridazines (7a-c, 8a-c) rather than the usual ethers (6a-c).Introduction of an electron-donating substituent into the 6-position of the pyridazine nucleus of 4 has been shown to suppress such telesubstitution processes.With phenyl-3-pyridazinylmethanol (3), thermally induced dismutation affording 3-benzylpyridazine (17) and 3-benzoylpyridazine (11) has been observed. Key Words: 3-Pyridazinylmethyl chlorides, reactions with O-nucleophiles / Telesubstitution / Dismutation, thermally induced

Preparation of Heteroaryl Phenylmethanes and a 13C and 15N NMR Spectroscopic Study of their Conjugate Carbanions. Rotational Isomerism and Charge Maps of the Anions and Ranking of the Charge Demands of the Heterocycles

2-Benzylpyridazine, 4-benzylpyrimidine, 2-benzylpyrimidine and 2-benzylpyrazine, (5-8) have been prepared in order to study their 13C and 15N spectra and those of their conjugate carbanions (1-4).These systems are aza-homologues of the previously reported

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.