13466-31-4

Basic information

• Product Name: Ethanone, 1-phenyl-, methylhydrazone
• CAS NO: 13466-31-4
• Molecular Formula: C9H12N2
• Molecular Weight: 148.208
• Mol File: 13466-31-4.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-phenyl-, methylhydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-phenyl-, methylhydrazone(13466-31-4)
• EPA Substance Registry System: Ethanone, 1-phenyl-, methylhydrazone(13466-31-4)

Safety Data

• Hazardous Substances Data: 13466-31-4(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 60-34-4 methylhydrazine 
• 536-74-3 phenylacetylene 
• 103-71-9 phenyl isocyanate 
• 6077-10-7 bis(phenylethynyl)mercury 

Downstream Products

• 76291-34-4 N-[1-{N-Methyl-N'-[1-phenyl-eth-(E)-ylidene]-hydrazino}-meth-(E)-ylidene]-methanesulfonamide 
• 1621003-27-7 (3R,4R,5R)-1,3-dimethyl-4-nitro-3,5-diphenylpyrazolidine 
• 3463-26-1 1-methyl-3-phenyl-1H-pyrazole 
• 1351960-16-1 (S)-2-dibenzylamino-propionic-N-phenylethylidene-N'-methylhydrazine 
• 3240-17-3 (α-Phenyl-aethylazo)-methan 
• 95642-86-7 C₁₁H₁₅N₃ 
• 135676-93-6 2,6-Dimethyl-5,6-diphenyl-1,2,5,6-tetrahydro-[1,2,4,5]tetrazine-3-carboxylic acid methyl ester 
• 135676-65-2 C₁₈H₂₀N₄O 
• 76291-45-7 4-Methyl-N-[1-{N-methyl-N'-[1-phenyl-eth-(Z)-ylidene]-hydrazino}-meth-(E)-ylidene]-benzenesulfonamide 
• 128364-63-6 (1-Methoxy-1-phenyl-ethyl)-methyl-diazene 
• 40093-30-9 C₁₄H₂₁N₃O 
• 40093-34-3 C₁₃H₁₉N₃O 
• 3240-18-4 α-Phenylaethyl-α-d-azomethan 

Relevant articles and documents

TEMPO-mediated Aza-diels-alder reaction: Synthesis of tetrahydropyridazines using ketohydrazones and olefins

A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem reaction of easily accessible ketohydrazones and olefins in the presence of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) has been successfully developed. The reaction involves the initial generation of azoalkenes from direct oxidative dehydrogenation of ketohydrazones using TEMPO as the commercially available oxidant, followed by a subsequent aza-Diels-Alder reaction with olefins.

Synthesis of a new class of bis(thiourea)hydrazide pseudopeptides as potential inhibitors of β-sheet aggregation

The modular synthesis of a novel pseudopeptide scaffold based on a bis(thiourea)hydrazide motif is reported. This compound class is designed to display "amphifinity", i.e. association with a peptide strand on one but not the other face of the scaffold, and hence could potentially inhibit β-sheet aggregation.

Rh(I) and Ir(I) catalysed intermolecular hydroamination with substituted hydrazines

The catalysed intermolecular hydroamination of a series of terminal alkynes with substituted hydrazines was achieved using Rh(i) and Ir(i) complexes.