55115-11-2

Usage

Usage

Intermediate in the synthesis of pharmaceuticals and agrochemicals

Biological activities

Anti-inflammatory and analgesic properties

Building block

In the synthesis of various heterocyclic compounds

Further research needed

To fully understand its properties and potential uses.

Upstream product

• 22706-20-3 5-methyl-2-phenyl-2H-tetrazole 
• 292638-85-8 acrylic acid methyl ester 
• 922-67-8 propynoic acid methyl ester 
• 103-02-6 acetone phenylhydrazone 
• 118559-38-9 N-(1-Nitroethylidene)-N'-phenyl-N'-sodiohydrazine 
• 55115-02-1 3-Methyl-1-phenyl-2-pyrazolin-5-carbonsaeure-methylester 
• 67-56-1 methanol 

Relevant academic research and scientific papers

1,3-Dipolar Cycloadditions, 88. C-Methyl-N-phenylnitrilimine and the Regiochemistry of its Cycloadditions

The title compound, a representative of the little known C-alkylnitrilimines, is accessible by three routes: NaNO2 elimination from sodium (α-nitroethylidene)phenylhydrazine in boiling acetonitrile, photolysis of 5-methyl-2-phenyltetrazole, and the thermo

ADDITION DE PHENYLHYDRAZONES AUX OLEFINES EN MILIEU NEUTRE

Phenylhydrazones may exhibit three types of reactivity towards alkenes: nucleophilic attack by carbon, nucleophilic attack by nitrogen and 1,3-dipolar cycloaddition through the azomethine imine ylide.The course of the reaction depends on the nature of the hydrazone and alkene substituents.