90861-42-0

Basic information

• Product Name: Ethanone, 1-phenyl-, (3-cyclohexyl-3-imino-1-phenyl-1-propenyl)hydrazone
• CAS NO: 90861-42-0
• Molecular Formula: C23H27N3
• Molecular Weight: 345.487
• Mol File: 90861-42-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-phenyl-, (3-cyclohexyl-3-imino-1-phenyl-1-propenyl)hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-phenyl-, (3-cyclohexyl-3-imino-1-phenyl-1-propenyl)hydrazone(90861-42-0)
• EPA Substance Registry System: Ethanone, 1-phenyl-, (3-cyclohexyl-3-imino-1-phenyl-1-propenyl)hydrazone(90861-42-0)

Safety Data

• Hazardous Substances Data: 90861-42-0(Hazardous Substances Data)

Upstream product

• 766-05-2 cyclohexane carbonitrile 
• 729-43-1 acetophenonazine 

Downstream Products

• 90861-63-5 4-Cyclohexyl-6-phenyl-1-[1-phenyl-eth-(E)-ylideneamino]-1H-pyrimidin-2-one 
• 90861-71-5 1-Amino-4-cyclohexyl-6-phenyl-1H-pyrimidin-2-one 
• 90861-56-6 [(E)-1-Cyclohexyl-3-phenyl-3-{N'-[1-phenyl-eth-(E)-ylidene]-hydrazino}-prop-2-en-(E)-ylidene]-carbamic acid ethyl ester 
• 90861-53-3 3-cyclohexyl-5-phenyl-1H-pyrazole 

Relevant articles and documents

Synthesis of Hydrazone Derivatives by Reaction of Azines with Nitriles, and Their Transformation into Pyrazoles and Pyrimidones

Reaction of equimolar amount of saturated nitriles and azines affords hydrazone derivatives; with unsymmetrical azines the reaction is regioselective and takes place with an alkyl substituent at the end of the azines opposite to an aryl substituent.Acid catalysed cyclisation and hydrolysis of the hydrazone derivatives yields N-unsubstituted pyrazoles, whereas aluminium chloride catalysed cyclisation of the N-ethoxycarbonyl analogues affords pyrimidones.