718-35-4

Basic information

• Product Name: 1-nitro-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene
• Synonyms: 1-nitro-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene
• CAS NO: 718-35-4
• Molecular Weight: 217.147
• Mol File: 718-35-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-nitro-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-nitro-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene(718-35-4)
• EPA Substance Registry System: 1-nitro-4-(3,3,3-trifluoroprop-1-en-1-yl)benzene(718-35-4)

Safety Data

• Hazardous Substances Data: 718-35-4(Hazardous Substances Data)

Upstream product

• 75-90-1 2,2,2-Trifluoroacetaldehyde 
• 2767-70-6 (p-nitrobenzyl)triphenylphosphonium bromide 
• 74031-42-8 (3,3,3-trifluoroprop-1-enyl)benzene 
• 21133-74-4 2-Chlor-3,3,3-trifluor-1-<4-nitro-phenyl>-propan 
• 21133-73-3 2-Brom-3,3,3-trifluor-1-<4-nitro-phenyl>-propan 
• 18583-39-6 (4-nitrobenzyl)triphenylphosphonium cation 
• 433-27-2 ethyl trifluoroacetaldehyde hemiacetal 
• 100-01-6 4-nitro-aniline 
• 937-31-5 (4-Nitrophenyl)acetylene 
• 619-89-6 p-nitrocinnamic acid 

Downstream Products

• 2338-84-3 1-(4-Hydroxy-phenyl)-2-(trifluormethyl)-ethylen 
• 49802-34-8 4-(3,3,3-trifluoropropyl)phenol 
• 3617-07-0 1-(1-bromo-3,3,3-trifluoropropyl)-4-nitrobenzene 
• 1983-15-9 4-(3,3,3-trifluoroprop-1-en-1-yl)aniline 

Relevant articles and documents

Deoxofluorination of (Hetero)aromatic Acids

Diverse trifluoromethyl-substituted compounds were synthesized by deoxofluorination of cinnamic and (hetero)aromatic carboxylic acids with sulfur tetrafluoride. The obtained products were used as starting materials in the preparation of novel fluorinated amino acids, anilines, and aliphatic amines - valuable building blocks for medicinal chemistry and agrochemistry.

Microwave-assisted preparation of trifluoroacetaldehyde (fluoral): isolation and applications

A novel method for the preparation of trifluoroacetaldehyde (fluoral, TFAc, CF3CHO) from commercially available trifluoroacetaldehyde ethylhemiacetal (TFAE) by microwave irradiation is described. The isolation, characterization and reaction of fluoral with various nucleophiles were studied to verify the diverse applicability of this new method.