74982-79-9

Basic information

• Product Name: 3,5-Pyridazinedicarbonitrile, 4-amino-1,6-dihydro-6-imino-1-(4-methylphenyl)-
• CAS NO: 74982-79-9
• Molecular Formula: C13H10N6
• Molecular Weight: 250.263
• Mol File: 74982-79-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3,5-Pyridazinedicarbonitrile, 4-amino-1,6-dihydro-6-imino-1-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Pyridazinedicarbonitrile, 4-amino-1,6-dihydro-6-imino-1-(4-methylphenyl)-(74982-79-9)
• EPA Substance Registry System: 3,5-Pyridazinedicarbonitrile, 4-amino-1,6-dihydro-6-imino-1-(4-methylphenyl)-(74982-79-9)

Safety Data

• Hazardous Substances Data: 74982-79-9(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 868-54-2 1,1,3-tricyano-2-amino-1-propene 
• 40257-94-1 2-[2-(4-methylphenyl)hydrazono]malononitrile 
• 109-77-3 malononitrile 
• 128755-93-1 3-Amino-2-cyano-4-(p-tolyl-hydrazono)-pent-2-enedinitrile 
• 96122-13-3 3-Amino-2-cyano-4-(p-tolyl-hydrazono)-pent-2-enedinitrile 

Relevant articles and documents

Synthesis of Polyfunctionally Substituted Pyridazines

The pyridazines 3,4,5, and 7 were obtained by reaction of the hydrazone derivatives 2 with several reagents.By treatment of 5 with acetic acid/hydrochloric acid, the pyrazolopyridazine 6 was formed.The pyrido-pyridazine derivatives 8 and 9 were obtained by reaction of 2 and 3 with malononitrile and ethyl cyanoacetate, respectively, and the isoxazolo-pyridazines 11 by reaction of 3a,b with hydroxylamine hydrochloride in ethanolic sodium ethoxide solution.The intermediate 9 was separated by reaction of 3a,b with hydroxylamine hydrochloride in ethanolic sodium acetate solution.

Reactions with the Arylhydrazones of α-Cyanoketones: Utility of Arylhydrazonomesoxalonitriles for the Synthesis of Azoles and Azolines

The arylhydrazonomesoxalonitriles derivatives 1 a-c were utilised for the synthesis of several new pyrimidine, pyridines, triazine and isoxazole derivatives.Compound 1a reacted with alkyl halides to yield the N-alkyl derivatives 12 a, b.The latter reacted