83015-28-5

Basic information

• Product Name: 1-BROMO-2-(1,1,2,2-TETRAFLUOROETHOXY)BENZENE
• Synonyms: 1-BROMO-2-(1,1,2,2-TETRAFLUOROETHOXY)BENZENE;1-BROMO-2-(TETRAFLUOROETHOXY)BENZENE;1-bromo-2-phenoxytetrafluoroethane
• CAS NO: 83015-28-5
• Molecular Formula: C₈H₅BrF₄O
• Molecular Weight: 273.02
• Mol File: 83015-28-5.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 211.1 °C at 760 mmHg
• Flash Point: 100.2 °C
• Appearance: /
• Density: 1.621 g/cm³
• CAS DataBase Reference: 1-BROMO-2-(1,1,2,2-TETRAFLUOROETHOXY)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-2-(1,1,2,2-TETRAFLUOROETHOXY)BENZENE(83015-28-5)
• EPA Substance Registry System: 1-BROMO-2-(1,1,2,2-TETRAFLUOROETHOXY)BENZENE(83015-28-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 83015-28-5(Hazardous Substances Data)

Usage

General Description

1-Bromo-2-(1,1,2,2-tetrafluoroethoxy)benzene is a complex organic compound that contains bromine, fluorine, oxygen, carbon, and hydrogen. Its molecular formula is C8H4BrF4O, indicating that it is made of 8 carbon atoms, 4 hydrogen atoms, 1 bromine atom, 4 fluorine atoms, and 1 oxygen atom. This chemical falls under the category of organo-bromine compounds and specifically under benzene and substituted derivatives. Due to the presence of the bromine atom, this compound may be used in bromination reactions in organic chemistry. Additionally, its fluorine content could suggest potential use in fluorochemical industry or fluorine chemistry. Although commercially valuable, it's critical to handle with caution due to potential toxicity and environmental impact.

Upstream product

• 124-73-2 1,2-dibromo-1,1,2,2-tetrafluoroethane 
• 100-67-4 potassium phenolate 
• 108-95-2 phenol 
• 139-02-6 sodium phenoxide 

Relevant articles and documents

Synthesis and Reactivity of Fluoroalkyl Copper Complexes by the Oxycupration of Tetrafluoroethylene

The copper(I)-mediated generation of -OCF2CF2- moieties by the oxycupration of tetrafluoroethylene (TFE) using either copper aryloxides or alkoxides is disclosed. The key intermediates, 2-aryloxy-1,1,2,2-tetrafluoroethyl and 2-alkoxy

Copper(0)-mediated fluoroalkylation of iodobenzene with 2-bromo-1,1,2,2-tetrafluoroethyl compounds: Investigation on the influence of R substituent on the reactivity of RCF2Cu species

We have made a systematic investigation on the copper(0)-mediated tetrafluoroethylenation of iodobenzene with structurally diverse 2-bromo-1,1,2,2-tetrafluoroethyl compounds. A comparison of this reaction with 1,2,2-trifluoro-1-phenylethylation and the known functionalized difluoroalkylation demonstrates that the substituent R of α,α-difluoroalkyl copper species RCF2Cu plays a crucial role on their reactivity, which is believed to be useful for the development of new fluoroalkylation reactions under the promotion of transition metals.

A practical synthesis of aryl tetrafluoroethyl ethers via the improved reaction of phenols with 1,2-dibromotetrafluoroethane

An efficient and practical synthesis of various aryl tetrafluoroethyl ethers by the reaction of phenols with 1,2-dibromotetrafluoroethane and the subsequent reduction with zinc dust was described. The nucleophilic substitution of 1,2-dibromotetrafluoroethane with phenols initiated by bromophilic attack was improved by using Cs2CO3 as a base and DMSO as a solvent.