772-53-2

Basic information

• Product Name: PHENYL TRIFLUOROVINYL ETHER
• Synonyms: PHENYL TRIFLUOROVINYL ETHER;[(Trifluorovinyl)oxy]benzene
• CAS NO: 772-53-2
• Molecular Formula: C₈H₅F₃O
• Molecular Weight: 174.12
• Mol File: 772-53-2.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 125.7°C at 760 mmHg
• Flash Point: 35.5°C
• Appearance: /
• Density: 1.248g/cm³
• Vapor Pressure: 14.6mmHg at 25°C
• Refractive Index: 1.454
• CAS DataBase Reference: PHENYL TRIFLUOROVINYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: PHENYL TRIFLUOROVINYL ETHER(772-53-2)
• EPA Substance Registry System: PHENYL TRIFLUOROVINYL ETHER(772-53-2)

Safety Data

• Hazardous Substances Data: 772-53-2(Hazardous Substances Data)

Usage

General Description

Phenyl trifluorovinyl ether, also known as 1,1,1,3,3,3-hexafluoro-2-phenoxy-1-propene, is a chemical compound with the molecular formula C9H5F6O. It is a colorless liquid with a fruity odor and is not soluble in water. Phenyl trifluorovinyl ether is primarily used as a reagent for organic synthesis, as a solvent for industrial processes, and as a component in specialty polymers. It is known for its high stability and resistance to heat, making it useful in high-temperature applications. However, it is important to handle this compound with care, as it can be hazardous to health and the environment.

InChI:InChI=1/C8H5F3O/c9-7(10)8(11)12-6-4-2-1-3-5-6/h1-5H

Upstream product

• 354-04-1 1,2-dibromo-1,1,2-trifluoroethane 
• 108-95-2 phenol 
• 116-14-3 polytetrafluoroethylene 
• 139-02-6 sodium phenoxide 
• 350-57-2 1,1,2,2-tetrafluoroethyl phenyl ether 
• 206667-03-0 C₉H₅F₄O₃^(1-)*K⁽¹⁺⁾ 
• 100-67-4 potassium phenolate 
• 1252017-26-7 2-phenoxytetrafluoropropionic acid 
• 83015-28-5 1,1,2,2-tetrafluoro-1-bromo-2-phenoxyethane 

Downstream Products

• 1427-46-9 C₁₆H₁₀F₆O₂ 
• 864715-99-1 2-bromo-1-(4-((trifluorovinyl)oxy)phenyl)propan-1-one 
• 1594970-70-3 C₈H₅ClF₈OS 

Relevant articles and documents

METHOD OF MAKING PERFLUOROCYCLOBUTANE-CONTAINING MONOMER

The invention pertains to a multi-step process for making polyfunctional aromatic compounds comprising two phenyl rings bearing reactive groups susceptible of polycondensation reaction to provide polycondensed polymers, said method using economic raw materials, and possessing high selectivity and overall yield.

Method for preparing trifluorovinyl aryl ether compound from dihalide trifluoroethane

The invention relates to a method for synthesizing a trifluorovinyl aryl ether compound, and belongs to the field of chemical synthesis. The dihalide trifluoroethane is taken as the starting material, reacts with a phenolic compound under proper conditions to synthesize the trifluorovinyl aryl ether compound. Compared with the traditional method, the provided synthesis method has the characteristics of mild reaction condition, simple operation, moderate yield and the like, has the advantages of simple process, low cost, low pollution and the like, and is expected to realize industrialized production.

Pentafluorosulfanyldifluoroacetic acid: Rebirth of a promising building block

Three novel, easily scalable routes for the synthesis of pentafluorosulfanyldifluoroacetic acid, SF5CF2C(O)OH, are described. Reactions of its acid chloride with amines and alcohols led to a small library of 15 amides and five esters