30410-39-0

Basic information

• Product Name: 3-phenyl-1-(p-tolyl)-2,3-diazaprop-2-en-1-one
• Synonyms: 3-phenyl-1-(p-tolyl)-2,3-diazaprop-2-en-1-one
• CAS NO: 30410-39-0
• Molecular Weight: 224.262
• Mol File: 30410-39-0.mol

Chemical Properties

• CAS DataBase Reference: 3-phenyl-1-(p-tolyl)-2,3-diazaprop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-phenyl-1-(p-tolyl)-2,3-diazaprop-2-en-1-one(30410-39-0)
• EPA Substance Registry System: 3-phenyl-1-(p-tolyl)-2,3-diazaprop-2-en-1-one(30410-39-0)

Safety Data

• Hazardous Substances Data: 30410-39-0(Hazardous Substances Data)

Upstream product

• 39719-02-3 N-Phenyl-N'-p-toluoylhydrazin 

Downstream Products

• 39719-02-3 N-Phenyl-N'-p-toluoylhydrazin 
• 92-52-4 biphenyl 
• 613-33-2 (4,4'-dimethyl-1,1'-biphenyl) 
• 644-08-6 4-Methylbiphenyl 
• 104-85-8 para-methylbenzonitrile 
• 1126669-33-7 (S)-5-ethyl-4,5-diphenyl-2-p-tolyl-4,5-dihydro-1,3,4-oxadiazin-6-one 
• 1126669-03-1 (R)-5-ethyl-4,5-diphenyl-2-p-tolyl-4,5-dihydro-1,3,4-oxadiazin-6-one 

Relevant articles and documents

Preparation of Blatter Radicals via Aza-Wittig Chemistry: The Reaction of N-Aryliminophosphoranes with 1-(Het)aroyl-2-aryldiazenes

Reacting N-aryliminophosphoranes with 1-(het)aroyl-2-aryldiazenes in preheated diphenyl ether at ca. 150-250 °C for 5-25 min affords in most cases the 1,3-diaryl-1,4-dihydrobenzo[e][1,2,4]triazin-4-yls (aka Blatter radicals) in moderate to good yields. Al

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A P(NMe2)3-mediated annulation reaction of N-Acyldiazenes with isothiocyanates, producing 2-imino-1,3,4-Thiadiazoles, is reported. This reaction proceeds well with crude N-Acyldiazenes derived from the oxidation of hydrazides by iodi

Thermolysis of polyazapentadienes. Part 10. Flash vacuum pyrolysis of azoalkenes and some azocarbonyl compounds

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