189442-95-3

Basic information

• Product Name: Ethanedione, (2-fluoro-4-pyridinyl)[3-(trifluoromethyl)phenyl]-, 1-oxime
• CAS NO: 189442-95-3
• Molecular Formula: C14H8F4N2O2
• Molecular Weight: 312.223
• Mol File: 189442-95-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanedione, (2-fluoro-4-pyridinyl)[3-(trifluoromethyl)phenyl]-, 1-oxime(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanedione, (2-fluoro-4-pyridinyl)[3-(trifluoromethyl)phenyl]-, 1-oxime(189442-95-3)
• EPA Substance Registry System: Ethanedione, (2-fluoro-4-pyridinyl)[3-(trifluoromethyl)phenyl]-, 1-oxime(189442-95-3)

Safety Data

• Hazardous Substances Data: 189442-95-3(Hazardous Substances Data)

Upstream product

• 116332-62-8 N-methoxy-N-methyl-3-trifluoromethylbenzamide 
• 2251-65-2 3-(Trifluoromethyl)benzoyl chloride 
• 76783-59-0 ethyl 3-(trifluoromethyl)benzoate 
• 461-87-0 2-fluoro-4-methylpyridine 

Downstream Products

• 189442-58-8 4-[5-(2-fluoropyridin-4-yl)-1-methyl-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]-piperidine-1-carboxylic acid benzyl ester 
• 234767-16-9 (S)-5-<2-(1-phenylethylamino)pyridin-4-yl>-4-<3-(trifluoromethyl)phenyl>-2-<4-(N-(benzyloxycarbonyl)piperidinyl)>imidazole 
• 189442-59-9 (S)-5-<2-(1-phenylethylamino)pyridin-4-yl>-1-methyl-4-<3-(trifluoromethyl)phenyl>-2-<4-(N-(benzyloxycarbonyl)piperidinyl)>imidazole 
• 189442-57-7 5-(2-fluoropyridin-4-yl)-4-<3-(trifluoromethyl)phenyl>-2-<4-(N-(benzyloxycarbonyl)piperidinyl)>imidazole 
• 189442-43-1 L-790,070 
• 913706-47-5 2-fluoro-4-[2-methylsulfanyl-5-(3-trifluoromethylphenyl)-3H-imidazol-4-yl]pyridine 
• 189442-56-6 4-[1-hydroxy-5-(2-fluoropyridin-4-yl)-4-(3-trifluoromethylphenyl)-1H-imidazol-2-yl]piperidine-1-carboxylic acid benzyl ester 

Relevant articles and documents

A concise and optimized four-step approach toward 2-(aryl-)alkylsulfanyl-, 4(5)-aryl-, 5(4)-heteroaryl-substituted imidazoles using alkyl- or arylalkyl thiocyanates

A convenient cyclization method leading to trisubstituted imidazoles in up to 84% yield is reported. Diverse 1-aryl-, 2-heteroaryl-substituted ethanones are converted into the corresponding α-oximino derivatives which are reduced under regioselective cond

An efficient synthesis of tetrasubstituted imidazoles from N-(2-Oxo)- amides

N-(2-Oxo)-amides were efficiently converted to tri- and tetra- substituted imidazoles under neutral reaction conditions upon treatment with neat ammonium trifluoroacetate.