61700-79-6

Basic information

• Product Name: Acetic acid, 2-(4-methylphenyl)hydrazide
• CAS NO: 61700-79-6
• Molecular Formula: C₉H₁₂N₂O
• Molecular Weight: 164.207
• Mol File: 61700-79-6.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 234.4°Cat760mmHg
• Flash Point: 92.4°C
• Density: 1.112g/cm³
• CAS DataBase Reference: Acetic acid, 2-(4-methylphenyl)hydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid, 2-(4-methylphenyl)hydrazide(61700-79-6)
• EPA Substance Registry System: Acetic acid, 2-(4-methylphenyl)hydrazide(61700-79-6)

Safety Data

• Hazardous Substances Data: 61700-79-6(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 108-24-7 acetic anhydride 
• 2028-84-4 p-methylbenzenediazonium chloride 
• 637-60-5 p-tolylhydrazine hydrochloride 
• 64-19-7 acetic acid 
• 57573-52-1 4-methylbenzene diazonium 
• 579-07-7 1-Phenylpropane-1,2-dione 
• 70638-39-0 2,5-dimethyl-2-p-tolylazo-furan-3-one 
• 431-03-8 dimethylglyoxal 
• 539-44-6 N-4-methylphenylhydrazine 

Downstream Products

• 681858-75-3 N,N'-dimethyl-N'-(4-methylphenyl)acetohydrazine 
• 36804-50-9 5-methyl-2,3-diphenyl-indole 
• 1616351-54-2 dimethyl 5-methyl-1-(p-tolyl)-1H-pyrazole-3,4-dicarboxylate 
• 1443787-39-0 N'-acetyl-N-(p-tolyl)isobutyrohydrazide 
• 1443787-37-8 N'-acetyl-2,4,6-trimethyl-N-(p-tolyl)benzohydrazide 
• 1443787-36-7 N'-acetyl-4-cyano-N-(p-tolyl)benzohydrazide 
• 1443787-38-9 N'-acetyl-N-(p-tolyl)acetohydrazide 
• 1443786-97-7 5-isopropyl-1-(p-tolyl)-1H-1,2,4-triazol-3-amine 
• 1443786-96-6 5-methyl-1-(p-tolyl)-1H-1,2,4-triazol-3-amine 
• 1443786-95-5 5-mesityl-1-(p-tolyl)-1H-1,2,4-triazol-3-amine 
• 1443786-94-4 5-(4-cyanophenyl)-1-(p-tolyl)-1H-1,2,4-triazol-3-amine 
• 1443786-93-3 5-(4-methoxyphenyl)-1-(p-tolyl)-1H-1,2,4-triazol-3-amine 
• 1443786-92-2 1,5-di-p-tolyl-1H-1,2,4-triazol-3-amine 
• 1443786-91-1 5-methyl-2,3-di-p-tolyl-1,3,4-oxadiazol-3-ium trifluoromethanesulfonate 

Relevant articles and documents

Synthesis of 2,3-dihydro-1H-indazoles by Rh(iii)-catalyzed C-H cleavage of arylhydrazines

A rhodium-catalyzed efficient method for the synthesis of 2,3-dihydro-1H-indazoles is described. The reaction of arylhydrazines with olefins results in the corresponding 2,3-dihydro 1H-indazoles with exclusive regioselectivity via C-H bond activation. The utility of the methodology is illustrated by a rapid synthesis of 1H-indazoles under mild reaction conditions in half an hour. This journal is the Partner Organisations 2014.

Indole synthesis by rhodium(III)-catalyzed hydrazine-directed C-H activation: Redox-neutral and traceless by N-N bond cleavage

Fishing for complements! There is an alternative to the useful Fischer indole synthesis. The new method utilizes the same retrosynthetic disconnection but is based on a RhIII-catalyzed directed C-H activation step and a successive coupling with alkynes. Copyright

Pyridoindolone derivatives substituted in the 3-position by a phenyl, their preparation and their application in therapeutics

The present invention relates to pyridoindolone derivatives substituted in the 3-position by a phenyl of general formula (I): to processes for preparing the same and to their use in therapeutics.