1422984-99-3

Basic information

• Product Name: (E)-(3,3,3-trifluoro-1-nitroprop-1-en-2-yl)benzene
• Synonyms: (E)-(3,3,3-trifluoro-1-nitroprop-1-en-2-yl)benzene
• CAS NO: 1422984-99-3
• Molecular Weight: 217.147
• Mol File: 1422984-99-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: (E)-(3,3,3-trifluoro-1-nitroprop-1-en-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-(3,3,3-trifluoro-1-nitroprop-1-en-2-yl)benzene(1422984-99-3)
• EPA Substance Registry System: (E)-(3,3,3-trifluoro-1-nitroprop-1-en-2-yl)benzene(1422984-99-3)

Safety Data

• Hazardous Substances Data: 1422984-99-3(Hazardous Substances Data)

Upstream product

• 434-45-7 2,2,2-Trifluoroacetophenone 
• 82945-27-5 2-nitro-1-trifluoromethyl-1-phenyl-1-ethanol 

Downstream Products

• 1422985-18-9 3,3,3-trifluoro-2-(1h-indol-3-yl)-2-phenylpropan-1-amine 
• 1422985-49-6 C₁₉H₁₇F₃N₂O 
• 1422985-47-4 1,4-diphenyl-4-(trifluoromethyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole 
• 1422985-48-5 1,4-diphenyl-4-(trifluoromethyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole 
• 1422985-19-0 3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-37-2 4-methoxy-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-38-3 5-methoxy-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-39-4 5-methyl-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-40-7 5-bromo-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-41-8 6-chloro-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-42-9 7-methyl-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1422985-43-0 (R)-2-methyl-3-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)-1H-indole 
• 1551094-52-0 4-(E)-methoxybenzaldehyde O-(2S)-(3-amino-1,1,1-trifluoro-2-phenylpropan-2-yl)oxime 
• 1551093-24-3 4-(E)-methoxybenzaldehyde O-(2S)-(1,1,1-trifluoro-3-nitro-2-phenylpropan-2-yl)oxime 

Relevant articles and documents

3-nitro-2-phenyl-2-(Trifluoromethyl)-2h-chromenes: Synthesis and reactions with nucleophiles

A method is proposed for the synthesis of 3-nitro-2-phenyl-2-(trifluoromethyl)-2H-chromenes by tandem condensation of salicylic aldehydes with (E)-3,3,3-trifluoro-1-nitro-2-phenylprop-1-ene in the presence of triethylamine. The example of 3-nitro-2-phenyl

Access to Chiral GABA Analogues Bearing a Trifluoromethylated All-Carbon Quaternary Stereogenic Center through Water-Promoted Organocatalytic Michael Reactions

Water enables the highly challenging enantioselective Michael addition of sterically congested β-trifluoromethyl-β-aryl- or -alkyl-substituted nitroolefins with dithiomalonates. Under on-water conditions, the reaction rates were remarkably accelerated as

Enantioselective Michael Addition of Pyrazolin-5-ones to β-CF3-β-Disubstituted Nitroalkenes Catalyzed by Squaramide Organocatalyst

A highly enantioselective Michael addition of pyrazolin-5-ones with β-CF3-β-disubstituted nitroalkenes catalyzed by bifunctional squaramide has been developed. Various chiral β-CF3-β-5-hydroxy-pyrazolin-3-yl-disubstituted nitroalkane derivatives bearing all-carbon quaternary stereocenter were prepared in good yields (up to 88%) and excellent enantioselectivities (up to 97% ee).