97675-21-3

Basic information

• Product Name: 1-(2-chloro-1,1,2-trifluoroethoxy)-4-methoxybenzene
• Synonyms: 1-(2-chloro-1,1,2-trifluoroethoxy)-4-methoxybenzene
• CAS NO: 97675-21-3
• Molecular Weight: 240.61
• Mol File: 97675-21-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(2-chloro-1,1,2-trifluoroethoxy)-4-methoxybenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-chloro-1,1,2-trifluoroethoxy)-4-methoxybenzene(97675-21-3)
• EPA Substance Registry System: 1-(2-chloro-1,1,2-trifluoroethoxy)-4-methoxybenzene(97675-21-3)

Safety Data

• Hazardous Substances Data: 97675-21-3(Hazardous Substances Data)

Upstream product

• 76-13-1 1,1,2-Trichloro-1,2,2-trifluoroethane 
• 1122-93-6 potassium p-methoxyphenolate 
• 79-38-9 Chlorotrifluoroethylene 
• 150-76-5 4-methoxy-phenol 

Relevant articles and documents

Base-catalyzed stereoselective hydrophenoxylation and hydrothiolation of hexafluorobutyne

Novel base-catalyzed hydrophenoxylation and hydrothiolation of hexafluorobutyne are described. By using an easily available base, a variety of vinyl ethers as well as sulfides are prepared at room temperature through two-phase nucleophilic addition reacti

Chemistry of Halogenoperfluoroalkanes> Synthesis of Fluorinated Ethers and Thioethers via Radical or Anionic Intermediates

Condensation of bromotrifluoromethane with potassium thiophenoxides in DMF is performed under pressure (2-3 atm) in a glass apparatus.Inhibition by nitrobenzene shows that a SRN1 mechanism is involved in the formation of aryl trifluoromethyl sulfides.Dichlorodifluoromethane itself reacts through a similar process to give aryl chlorodifluoromethyl sulfides.Condensation of 1,1,2-trichlorotrifluoroethane with potassium thiophenoxide or phenoxide occurs even in the presence of nitrobenzene.The formation of aryl 2,2-dichloro-1,1,2-trifluoroethyl sulfides or ethers can be explained by a chain carbanionic mechanism.