88254-46-0

Usage

Common uses

Reagent in organic synthesis, potential precursor for nitrogen-containing compounds

Properties

Versatile, potential anti-tumor agent, chelating agent for heavy metal ions

Applications

Inhibiting growth of cancer cells, intermediate in pharmaceutical and agrichemical production

Upstream product

• 1073-70-7 4-chlorophenylhydrazine hydrochloride 
• 104-55-2 3-phenyl-propenal 
• 14371-10-9 (E)-3-phenylpropenal 
• 1073-69-4 N-4-chlorophenylhydrazine 

Downstream Products

• 88246-36-0 (4-Chloro-phenyl)-[(E)-3-phenyl-3-(4,5,6,7-tetrahydro-benzo[1,3]dithiol-2-ylidene)-propenyl]-diazene 
• 1586799-58-7 4-benzyl-6-chlorocinnoline 

Relevant academic research and scientific papers

Aluminium chloride-catalyzed synthesis of 4-benzyl cinnolines from aryl hydrazones

An efficient synthesis of 4-benzyl cinnolines from aryl phenylallylidene hydrazone is described. In this report aluminium chloride as a Lewis acid catalyst and toluene as a solvent are used for the synthesis. This method is expected to more advantageous t

Preparation and Absorption Spectra of Arylhydrazones from α,β-Unsaturated Carbonyl Compounds

Substituted arylhydrazones 2-17, 19, and 23-29 were prepared from several α,β-unsaturated carbonyl compounds and their absorption spectra examined.The dependence on concentration of certain near-infrared bands of the spectra has been associated with aggregation and appears to correlate with structural elements of the compounds in a way suggesting significant intermolecular effects, either hydrogen bonding or charge transfer of both.