59803-60-0

Upstream product

• 124-41-4 sodium methylate 
• 15878-17-8 5-chloro-3-phenyl-1H-pyrazole 
• 80-48-8 methyl p-toluene sulfonate 
• 77-78-1 dimethyl sulfate 
• 141-52-6 sodium ethanolate 
• 74-88-4 methyl iodide 
• 10562-42-2 3,3-dichloro-1-phenyl-propenone 
• 57-14-7 N,N-Dimethylhydrazine 
• 80030-92-8 2-methyl-5-phenyl-2,3-dihydro-1H-pyrazol-3-one 
• 41927-50-8 1-methyl-3-phenyl-2-pyrazolin-5-one 

Downstream Products

• 91411-70-0 4-bromo-5-chloro-1-methyl-3-phenyl-1H-pyrazole 
• 59803-61-1 3-chloro-1,2-dimethyl-5-phenylpyrazolium iodide 
• 59803-75-7 3-chloro-1,2-dimethyl-5-phenylpyrazolium methyl sulfate 
• 76439-32-2 1-(1-methyl-5-phenyl-3-pyrazolyl)piperidine 
• 76439-37-7 3-methyl-1-(1-methyl-5-phenyl-3-pyrazolyl)piperidine 
• 76439-39-9 1-(1-methyl-3-phenyl-5-pyrazolyl)piperidine 
• 76439-38-8 3-methyl-1-(1-methyl-3-phenyl-5-pyrazolyl)piperidine 
• 76439-33-3 4-Methoxy-1-(1-methyl-5-phenyl-1H-pyrazol-3-yl)-piperidine 
• 65404-61-7 1,2-dimethyl-3-(3-methylpiperidino)-5-phenylpyrazolium chloride 
• 65404-60-6 1,2-dimethyl-3-(3-methylpiperidino)-5-phenylpyrazolium methyl sulfate 
• 883-38-5 5-chloro-1-methyl-3-phenyl-1H-pyrazole-4-carboxaldehyde 

Relevant academic research and scientific papers

New synthesis and properties of 3-alkyl-, 3-chloroalkyl-, 3-perfluoroalkyl-, and 3-aryl-1-methyl-(5-halo)pyrazoles from chloro(bromo) vinyl ketones and N,N-dimethylhydrazine

A new regioselective heterocyclization was revealed in the reaction of 2-chloro- and 2,2-dichloro-(bromo)vinyl ketones with N,N-dimethylhydrazine to afford 3-substituted 1-methyl(5-halo)pyrazoles. The reaction is accompanied by elimination of methyl halide and formation of up to 90% of N,N,N-trimethylhydrazinium halide as the second product.

Novel 1,2-dialkylpyrazolium compounds having 3-(or 3,5-) nitrogen-containing heterocyclic group as herbicides

There are provided 1,2-dialkylpyrazolium compounds having positioned thereon a 3- or 5-substituted nitrogen-containing heterocyclic group or 3,5-disubstituted nitrogen-containing heterocyclic groups as well as a method for preparing the same. There is als

1,2-Dialkyl-3(or 3,5)-N-heterocyclic pyrazolium salts of derivatives thereof as fungicidal agents

There is provided a method for controlling fungi with a fungicidally effective amount of a 1,2-dialkyl-3(or 3,5)-N-heterocyclic pyrazolium salt. There is also provided a method for protecting living plants from attack by fungi through the application to t

3,5-Cycloalkyl pyrazolium salts as fungicides

There is provided a method for the control of plant pathogenic fungi with certain 3(5) or 3,5-cycloalkyl pyrazolium salts and to a method of protecting plants from fungal attack by applying to the foliage of said plants said pyrazolium salt in fungicidall

Novel 3 or 5-aminopyrazolium salts and fungicidal use thereof

There are provided certain novel 1,2-dimethyl pyrazolium compounds having nitrogen containing substituents in the 3 or 5 position, and to both a method for controlling plant pathogenic fungi with said compounds and a method for protecting plants from an a