905-79-3

Basic information

• Product Name: Phenyl--keton-p-tosylhydrazon
• Synonyms: Phenyl--keton-p-tosylhydrazon
• CAS NO: 905-79-3
• Molecular Weight: 351.429
• Mol File: 905-79-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Phenyl--keton-p-tosylhydrazon(CAS DataBase Reference)
• NIST Chemistry Reference: Phenyl--keton-p-tosylhydrazon(905-79-3)
• EPA Substance Registry System: Phenyl--keton-p-tosylhydrazon(905-79-3)

Safety Data

• Hazardous Substances Data: 905-79-3(Hazardous Substances Data)

Upstream product

• 91-02-1 phenyl(pyridin-2-yl)methanone 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 

Downstream Products

• 1384956-04-0 (E)-7-(1,2-diphenylvinyl)-3-phenyl-[1,2,3]triazolo[1,5-a]pyridine 
• 1384956-13-1 (E)-7-(hex-3-en-3-yl)-3-phenyl-[1,2,3]triazolo[1,5-a]pyridine 
• 1384956-14-2 (E)-7-(oct-4-en-4-yl)-3-phenyl-[1,2,3]triazolo[1,5-a]pyridine 
• 1384956-15-3 (E)-7-(4-methylpent-2-en-2-yl)-3-phenyl-[1,2,3]triazolo[1,5-a]pyridine 
• 832-81-5 3-phenyl-[1,2,3]triazolo[1,5-a]pyridine 

Relevant articles and documents

Ni-catalyzed alkenylation of triazolopyridines: Synthesis of 2,6-disubstituted pyridines

A synthetic strategy to access 2,6-disubstituted pyridines from triazolopyridines through a regioselective nickel-catalyzed alkenylation reaction of the C7-H bond is described. The N2 fragment embedded in the resulting C-H functionalized triazolopyridine can be readily excised using acidic or oxidative conditions to unmask the pyridine.

Synthesis and structural characterization of arene d6 metal complexes of sulfonohydrazone and triazolo ligands: High potency of triazolo derivatives towards DNA binding

Complexation of [(p-cymene)RuCl2]2 and [Cp?MCl2]2 (M = Rh/Ir) with chelating ligand 4-methylbenzenesulfonohydrazone ligands (L1 and L3) resulted in the formation of mononuclear cationic complexes having PF6