380-78-9 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-1,1,2-TRIFLUOROETHYL ETHYL ETHER is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its reactivity with multiple types of compounds allows for the creation of a wide range of medicinal agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-1,1,2-TRIFLUOROETHYL ETHYL ETHER is utilized as an intermediate in the production of agrochemicals, contributing to the development of pesticides and other agricultural products.
Used in Organic Synthesis:
2-BROMO-1,1,2-TRIFLUOROETHYL ETHYL ETHER is employed as a reagent in organic synthesis, where its ability to react with a variety of compounds is leveraged to form complex organic molecules.
Used as a Solvent in Chemical Reactions:
2-BROMO-1,1,2-TRIFLUOROETHYL ETHYL ETHER is used as a solvent in various chemical processes, facilitating reactions that require a suitable liquid medium.
Used as a Propellant in Aerosol Products:
2-BROMO-1,1,2-TRIFLUOROETHYL ETHYL ETHER also serves as a propellant in aerosol products, providing the force necessary to dispense the product from its container.
Check Digit Verification of cas no
The CAS Registry Mumber 380-78-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 380-78:
(5*3)+(4*8)+(3*0)+(2*7)+(1*8)=69
69 % 10 = 9
So 380-78-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H6BrF3O/c1-2-9-4(7,8)3(5)6/h3H,2H2,1H3
380-78-9Relevant academic research and scientific papers
Tetrafluorine-containing ketones and acetoacetates: Synthesis and mechanistic study
Tsai, Hou-Jen,Hsieh, Chi-Wei
, p. 749 - 757 (2008/03/11)
Addition of trimethylsilyl trifluoroacetate to the carbanions of α-fluorobenzyl-phosphonate (3) or diisopropyl(fluorocarbethoxymethyl) phosphonate (9) formed the corresponding intermediates [CF3C(O)CFPh] -Li+ (10) and [CF3C(O)CFCO2Et] -Li+ (11), respectively. Subsequent protonation, alkylation or allylation of 10 and 11 afforded trifluoromethyl fluorobenzyl ketones 12 and ethyl 2,4,4,4-tetra-fluoroacetoacetates 13. Based on the results obtained, a plausible mechanism was proposed.
OBSERVATION OF A COMPETITIVE PATH IN THE NUCLEOPHILIC ADDITION OF FLUOROOLEFINS: THE BROMOPHILIC REACTION OF THE ADDUCT CARBANOIN INTERMEDIATE
Jiang, Xi-Kui,Ji, Guo-Znen,Shi,Yi-Qun
, p. 405 - 418 (2007/10/02)
In addition to the hydro-alkoxy-addition products ROCF2CFBrH (4), and olefin products ROCF=CFBr (5), a new type of product, i.e., the alkoxy-bromo-addition products ROCF2CFBr2 (6) have been obtained in the reactions of bromotrifluoro-ethene (3) with different alkoxides (RO- = t-BuO=, i-PrO-, EtO- and MeO-).These products (6) are formed from a competitive path involving bromophilic reactions of the intermediate adduct carbanions (8).Radicals have been shown to be unlikely intermediates of this competitive reaction path.
