64252-53-5

Basic information

• Product Name: Ethanone, 1-(4-methylphenyl)-, hydrazone
• Synonyms: 1-p-Tolyl-aethanon-hydrazon;4-methylacetophenone hydrazone;p-methylacetophenone hydrazone;4-Methyl-acetophenon-hydrazon;1-p-tolyl-ethanone-hydrazone
• CAS NO: 64252-53-5
• Molecular Formula: C9H12N2
• Molecular Weight: 148.208
• Mol File: 64252-53-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(4-methylphenyl)-, hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(4-methylphenyl)-, hydrazone(64252-53-5)
• EPA Substance Registry System: Ethanone, 1-(4-methylphenyl)-, hydrazone(64252-53-5)

Safety Data

• Hazardous Substances Data: 64252-53-5(Hazardous Substances Data)

Upstream product

• 122-00-9 para-methylacetophenone 
• 766-97-2 4-n-methylphenylacetylene 
• 5757-88-0 p-Methylacetophenone N,N-dimethylhydrazone 

Downstream Products

• 622-96-8 4-methylethylbenzene 
• 122-00-9 para-methylacetophenone 
• 452335-62-5 1-(1,1-dibromoprop-1-en-2-yl)-4-methylbenzene 
• 1200687-97-3 2,5-bis(4-cyanophenyl)tellurophene 
• 1200687-99-5 2,5-bis(4-nitrophenyl)tellurophene 
• 64252-52-4 1-(1-diazoethyl)-4-methylbenzene 
• 89752-30-7 7-Methyl-2,3a,5-triphenyl-7-p-tolyl-3,3a-dihydro-pyrazolo[1,5-c][1,3]oxazine 
• 103-89-9 4-Methylacetanilide 
• 74331-86-5 (E)-1,2-Dibromo-1-(4-methylphenyl)ethylene 
• 74346-16-0 (Z)-1,2-Dibromo-1-(4-methylphenyl)ethylene 
• 619-41-0 4-(bromoacetyl)toluene 

Relevant articles and documents

Exploring the Influence of Phosphine Ligation on the Gold-Catalyzed Hydrohydrazination of Terminal Alkynes at Room Temperature

The synthesis and/or NMR/X-ray characterization of a new series of (L)AuCl complexes is reported, featuring BippyPhos, AdJohnPhos, silyl ether based ligands including OTips-DalPhos, and PAd-DalPhos. These complexes, along with previously reported analogue

Sulphur promoted C(sp3)-C(sp2) cross dehydrogenative cyclisation of acetophenone hydrazones with aldehydes: Efficient synthesis of 3,4,5-trisubstituted 1H-pyrazoles

A novel strategy for the cross dehydrogenative coupling (CDC) of acetophenone hydrazones and aldehydes has been developed for the synthesis of highly substituted pyrazoles. This work, for the first time, uses elemental sulfur as a promoter as well as a hydrogen acceptor in effecting the Csp3-Csp2 bond formation via C-H activation. This journal is

Room-temperature hydrohydrazination of terminal alkynes catalyzed by saturated abnormal n-heterocyclic carbene-gold(I) complexes

A number of saturated abnormal N-heterocyclic carbene (NHC) complexes of gold, in combination with KBArF4 as activator, were successfully applied in the chemoselective addition of hydrazine to alkynes. The reaction proceeds even at r