116853-79-3

Basic information

• Product Name: Acetaldehyde, trifluoro-, (4-methoxyphenyl)hydrazone
• CAS NO: 116853-79-3
• Molecular Formula: C9H9F3N2O
• Molecular Weight: 218.178
• Mol File: 116853-79-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Acetaldehyde, trifluoro-, (4-methoxyphenyl)hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Acetaldehyde, trifluoro-, (4-methoxyphenyl)hydrazone(116853-79-3)
• EPA Substance Registry System: Acetaldehyde, trifluoro-, (4-methoxyphenyl)hydrazone(116853-79-3)

Safety Data

• Hazardous Substances Data: 116853-79-3(Hazardous Substances Data)

Upstream product

• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 3471-32-7 4-Methoxyphenylhydrazine 
• 421-53-4 2,2,2-trifluoro-1,1-ethanediol 
• 19501-58-7 4-methoxyphenylhydrazine hydrochloride 
• 99333-34-3 N-(2,2,2-trifluoroethylidene)-4-methoxyaniline 

Downstream Products

• 188817-13-2 SC-560 
• 1617533-11-5 4-isopropyl-1-(4-methoxyphenyl)-3-(trifluoromethyl)-1,4-dihydropyridazine 
• 630382-44-4 1-(4-methoxyphenyl)-3-(trifluoromethyl)-5,6-dihydro-1H-pyrazolo[3,4-c]pyridin-7(4H)-one 
• 139285-32-8 4-Methoxy-1-(4-methoxy-phenyl)-5-methyl-3-trifluoromethyl-1H-pyrazole 
• 139285-25-9 4-hydroxy-1-(p-methoxyphenyl)-5-methyl-3-trifluoromethylpyrazole 

Relevant articles and documents

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

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

Trifluoromethylated 2,3-dihydro-1,3,4-thiadiazoles via the regioselective [3+2]-cycloadditions of fluorinated nitrile imines with aryl, hetaryl, and ferrocenyl thioketones

A series of hydrazonoyl bromides prepared from readily available N-arylhydrazones of fluoral was used for the in situ generation of fluorinated nitrile imines. These 1,3-dipoles were efficiently trapped with aryl and hetaryl thioketones yielding fluoromet