98664-40-5

Basic information

• Product Name: N-(4-methylphenyl)trifluoroacetohydrazonoyl bromide
• Synonyms: N-(4-methylphenyl)trifluoroacetohydrazonoyl bromide
• CAS NO: 98664-40-5
• Molecular Weight: 281.075
• Mol File: 98664-40-5.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: N-(4-methylphenyl)trifluoroacetohydrazonoyl bromide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-methylphenyl)trifluoroacetohydrazonoyl bromide(98664-40-5)
• EPA Substance Registry System: N-(4-methylphenyl)trifluoroacetohydrazonoyl bromide(98664-40-5)

Safety Data

• Hazardous Substances Data: 98664-40-5(Hazardous Substances Data)

Upstream product

• 637-60-5 p-tolylhydrazine hydrochloride 
• 539-44-6 N-4-methylphenylhydrazine 
• 98664-42-7 trifluoroacetaldehyde 4-methylphenylhydrazone 

Downstream Products

• 524699-80-7 2,2,2-trifluoro-N'-(p-tolyl)acetohydrazonamide 
• 1293294-80-0 2-(1-(p-tolyl)-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl)pyridine 
• 1293294-91-3 2-methyl-5-(5-(pyridin-2-yl)-3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl)benzene-1-sulfonyl chloride 
• 1293294-82-2 2-methyl-5-(5-(pyridin-2-yl)-3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl)benzenethiol 
• 1293293-84-1 2-(1-(4-methyl-3-(2,2,2-trifluoroethylthio)phenyl)-3-(trifluoromethyl)-1H-1,2,4-triazol-5-yl)pyridine 

Relevant articles and documents

A straightforward access to 3-trifluoromethyl-1H-indazoles via (3+2)-cycloaddition of arynes with nitrile imines derived from trifluoroacetonitrile

In situ generated arynes react with nitrile imines derived from trifluoroacetonitrile at 0 °C in THF solutions yielding 3-trifluoromethyl-1H-indazole derivatives as the only intermolecular products. The reaction corresponds the expected (3 + 2)-cycloaddit

Novel trifluoromethylated spiro-1,3,4-thiadiazoles via [3+2]-cycloadditions of 2,3-diphenylcyclopropenethione with selected in situ-generated nitrile imines derived from trifluoroacetonitrile

The in situ-generated N-aryl nitrile imines derived from trifluoroacetonitrile react efficiently with 2,3-diphenylcyclopropenethione to give spirocyclic 1,3,4-thiadiazole derivatives as products of a regio- and chemoselective [3+2]-cycloaddition in good t

Polysubstituted 3-trifluoromethylpyrazoles: Regioselective (3 + 2)-cycloaddition of trifluoroacetonitrile imines with enol ethers and functional group transformations

Non-catalysed addition of trifluoroacetonitrile imines to enol ethers provided fully regioselectively (3 + 2)-cycloadducts, which either spontaneously or via Br?nsted acid-induced elimination of ROH molecules led to the formation of 3-trifluoromethylated