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Catalog Number:
36911
CAS Number:
425-75-2
Trifluorométhanesulfonate d'éthyle
Purity:
≥ 98% (CG)
Synonym(s):
Ester éthylique de l'acide trifluorométhanesulfonique, Triflate d'éthyle
Hazmat
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$29.34 /1G
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Product Information

Ethyl trifluoromethanesulfonate is a versatile and highly reactive sulfonate ester that serves as a valuable reagent in organic synthesis. Known for its trifluoromethyl group, this compound is particularly useful in the introduction of trifluoromethyl groups into various organic molecules, enhancing their biological and chemical properties. It is widely utilized in the pharmaceutical industry for the development of novel drug candidates, as well as in agrochemicals for the synthesis of effective pesticides and herbicides. Its ability to facilitate the formation of carbon-fluorine bonds makes it an essential tool for researchers aiming to create compounds with improved stability and bioactivity.

In addition to its applications in pharmaceuticals and agrochemicals, ethyl trifluoromethanesulfonate is also employed in materials science for the modification of polymers and in the development of advanced materials with unique properties. Its high reactivity and selectivity allow for efficient transformations, making it a preferred choice among chemists. With its growing importance in various fields, ethyl trifluoromethanesulfonate continues to be a compound of interest for researchers and industry professionals alike.

Synonyms
Ester éthylique de l'acide trifluorométhanesulfonique, Triflate d'éthyle
CAS Number
425-75-2
Purity
≥ 98% (CG)
Molecular Formula
C3H5F3O3S
Molecular Weight
178.13
MDL Number
MFCD00000410
PubChem ID
67924
Density
1.374
Appearance
Liquide incolore à jaune clair
Boiling Point
114 - 116 °C
Refractive Index
1.336
Conditions
Magasin chez RT
General Information
Synonyms
Ester éthylique de l'acide trifluorométhanesulfonique, Triflate d'éthyle
CAS Number
425-75-2
Purity
≥ 98% (CG)
Molecular Formula
C3H5F3O3S
Molecular Weight
178.13
MDL Number
MFCD00000410
PubChem ID
67924
Density
1.374
Appearance
Liquide incolore à jaune clair
Boiling Point
114 - 116 °C
Refractive Index
1.336
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl trifluoromethanesulfonate is widely utilized in research focused on:

  • Fluorination Reactions: This compound serves as a potent fluorinating agent, enabling the introduction of fluorine into organic molecules, which is crucial in pharmaceuticals and agrochemicals for enhancing biological activity.
  • Building Block in Synthesis: It acts as a versatile building block for synthesizing complex molecules, particularly in the development of new materials and specialty chemicals, making it invaluable in the chemical industry.
  • Reagent in Organic Chemistry: Researchers use it as a reagent for various organic transformations, including nucleophilic substitutions, which can lead to the creation of novel compounds with desirable properties.
  • Development of Fluorinated Compounds: Its application in producing fluorinated compounds is significant in creating materials with unique properties, such as increased stability and lower reactivity, which are essential in high-performance applications.
  • Environmental Applications: Ethyl trifluoromethanesulfonate is explored for use in developing environmentally friendly solvents and reagents, addressing the industry's need for sustainable chemical processes.

Citations