380-44-9

Basic information

• Product Name: ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER
• Synonyms: 2-CHLORO-1,1,2-TRIFLUOROETHYL ALLYL ETHER;6-CHLORO-5,5,6-TRIFLUORO-4-OXAHEXENE;ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER
• CAS NO: 380-44-9
• Molecular Formula: C5H6ClF3O
• Molecular Weight: 174.55
• Mol File: 380-44-9.mol

Chemical Properties

• Boiling Point: 109.2 °C
• Flash Point: 24.2°C
• Appearance: /
• Density: 1.25
• Vapor Pressure: 21.7mmHg at 25°C
• Refractive Index: 1.369
• CAS DataBase Reference: ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER(380-44-9)
• EPA Substance Registry System: ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER(380-44-9)

Safety Data

• Hazard Codes: Xi
• Statements: 10
• Safety Statements: 16
• RIDADR: 3271
• HazardClass: IRRITANT
• Hazardous Substances Data: 380-44-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER is used as an intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines. Its unique properties make it a valuable component in the production process.
Used in Agrochemical Industry:
In the agrochemical sector, ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER is utilized as an intermediate in the creation of agrochemicals, which are essential for enhancing crop protection and yield.
Used in Organic Synthesis:
ALLYL 2-CHLORO-1,1,2-TRIFLUOROETHYL ETHER is employed as a solvent and reagent in organic synthesis, facilitating various chemical reactions and contributing to the formation of complex organic molecules.
Used in Research and Development:
This chemical compound is also used in research and development settings for exploring new chemical reactions and developing innovative applications in various industries, underlining its importance in scientific advancement.

InChI:InChI=1/C5H6ClF3O/c1-2-3-10-5(8,9)4(6)7/h2,4H,1,3H2

Upstream product

• 79-38-9 Chlorotrifluoroethylene 
• 107-18-6 allyl alcohol 

Downstream Products

• 731-20-4 Dichlor-<3-(1.1.2-trifluor-2-chlor-ethoxy)-propyl>-phenyl-silan 

Relevant articles and documents

TRANSFORMATION D'OXYDES D'ALKYLES ET DE POLYFLUOROALKYLES PAR LES ACIDES DE LEWIS. INFLUENCE DES RADICAUX ALKYLES.

The generation of perfluoroalkanoyl fluorides from perfluoroalkyl ethers by Lewis acids RHOCF2RF -> FRH + RFCOF depends mainly upon the nature of the alkyl RH radical.It is necessary to use RH groups with donor character and also electrophilic groups present on the radicals can facilitate the breaking of the RH-O bond.As examples, ethers with Me3SiCH2CH2 or CH2=CH-CH2 groups allowed reactions to occur readily at room temperature or below using common Lewis acids such as ZnCl2, BF3-Et2O, AlCl3.