354-51-8

Basic information

• Product Name: 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane
• Synonyms: 1,2-dibromo-1-chloro-1,2,2-trifluoro-ethan;1,2-dibromo-2-chloro-1,1,2-trifluoroethane;1,2-Dibromo-2-chloro-1,1,2-trifluroethane;1,2-Dibromochlorotrifluoroethane;1,2-Dibromotrifluorochloroethane;1-Chloro-1,2-dibromotrifluoroethane;CFC-1132alphaAE;Ethane, 1,2-dibromo-1-chloro-1,2,2-trifluoro-
• CAS NO: 354-51-8
• Molecular Formula: C₂Br₂ClF₃
• Molecular Weight: 276.28
• EINECS: 206-562-5
• Product Categories: organofluorine compounds
• Mol File: 354-51-8.mol
• Article Data: 10

Chemical Properties

• Melting Point: -72,9°C
• Boiling Point: 93-94°C
• Flash Point: 9.1 °C
• Appearance: colorless/liquid
• Density: 2,248 g/cm3
• Vapor Pressure: 60.8mmHg at 25°C
• Refractive Index: 1.4275
• CAS DataBase Reference: 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane(354-51-8)
• EPA Substance Registry System: 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane(354-51-8)

Safety Data

• Hazard Codes: Xi
• RTECS: KH9300000
• HazardClass: IRRITANT
• Hazardous Substances Data: 354-51-8(Hazardous Substances Data)

Usage

General Description

1,2-Dibromo-1-chloro-1,2,2-trifluoroethane is a chemical compound that is commonly used as a refrigerant and as a solvent for cleaning electronic equipment. It is also known by its trade name, Halon 123. 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane is a colorless, heavy liquid with a slightly sweet odor, and it is highly volatile. It is also non-flammable, making it a popular choice for fire extinguishing agents. However, it has been found to be an ozone-depleting substance and has been largely phased out of use due to its harmful effects on the environment. Additionally, chronic exposure to 1,2-Dibromo-1-chloro-1,2,2-trifluoroethane can cause damage to the liver, kidneys, and central nervous system in humans.

InChI:InChI=1/C2Br2ClF3/c3-1(5,6)2(4,7)8

Upstream product

• 354-54-1 1-chloro-1-iodo-2-bromo-1,2,2-trifluoroethane 
• 79-38-9 Chlorotrifluoroethylene 
• 7726-95-6 bromine 
• 359-11-5 1,1,2-trifluoroethylene 

Downstream Products

• 378-13-2 1,4-dibromo-2-chloro-1,1,2-trifluorobutane 
• 358-27-0 1,6-dibromo-2-chloro-1,1,2,4,6-pentafluoro-hexane 
• 428-77-3 1,6-dibromo-2-chloro-1,1,2,4,4,6,6-heptafluoro-hexane 
• 359-11-5 1,1,2-trifluoroethylene 
• 380-57-4 2-chloro-1,4-dibromo-1,1,2-trifluoropentane 
• 380-58-5 1,4-dibromo-2-chloro-1,1,2,4-tetrafluoro-butane 
• 558-57-6 1,2-dibromo-1,1-dichloro-2,2-difluoroethane 
• 758-24-7 1-Bromo-1-chloro-2,2-difluoroethylene 
• 666-19-3 1,2-dibromo-1-chloro-2-fluoro-ethene 
• 754-17-6 1-chloro-1,1-dibromotrifluoroethane 
• 375-42-8 1,4-dibromo-2,3-dichloro-1,1,2,3,4,4-hexafluorobutane 
• 85131-86-8 1,6-Dibromo-2,3,5-trichloro-1,1,2,3,4,4,5,6,6-nonafluorohexane 
• 95519-56-5 (2,2-Dibromo-1,1,2-trifluoro-ethoxy)-benzene 
• 456-62-2 1-hydro-1-chloro-2-phenoxyperfluoroethane 

Relevant articles and documents

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Method for synthesizing 4 -halo -1, 1 and 2 -trifluoro -1 -butene (by machine translation)

The invention discloses a method for synthesizing 4 -halo -1, 1 and 2 -trifluoro -1 -butene. , Polyhaloethane is synthesized by reaction of chlorotrifluoroethylene with halogen, and then polyhalogenated ethane is reacted with ethylene under the action of a catalyst to synthesize polyhalogenated butane, and finally, 4 - halogenated -1, 1 and 2 -trifluoro -1 -butene are dehalogenated under the action of a reducing agent. The method has the characteristics of simple synthesis method, high product purity and low preparation cost. (by machine translation)

CHEMICAL PRODUCTION PROCESSES AND SYSTEMS

Chemical production processes are provided that include reacting a metal comprising olefin to form a conjugated olefin; reacting a heterohalogenated olefin to form a conjugated olefin; reacting a halogenated alkane to form a conjugated olefin; and/or reacting a hydrohalogenated olefin to form a conjugated olefin. Chemical production systems are also provided that can include: a first reactant reservoir configured to house a perhalogenated olefin; a second reactant reservoir configured to house a catalyst mixture; a first reactor coupled to both the first and second reservoirs, the first reactor configured to house a metal-comprising mixture and receive both the perhaloganated olefin form the first reactant reservoir and the reactant mixture from the second reactant reservoir; and a product collection reservoir coupled to the first reactor and configured to house a conjugated olefin.

Bromosulphonated fluorinated cross-linkabke elastomers based on vinylidene fluoride having low t9 and processes for their preparation

Compounds corresponding to formula (I) F2C═CFX(CY2)nBr??(I) in which: X represents an atom of oxygen or no atom; Y represents an atom of hydrogen or of fluorine; and n is a whole natural number ranging from 0 to 10 inclusive, excluding bromotrifluoroethylene, 3-bromo-perfluoropropene, 4-bromo-1,1,2,-trifluorobutene, 4-bromo-perfluorobutene-1 and perfluoro(2-bromo-ethylvinyl ester), and their use in the synthesis of fluorinated copolymers then in the synthesis of homosulphonated fluorinated elastomers, exhibiting a low glass transition temperature.