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Catalog Number:
31485
CAS Number:
6226-25-1
Trifluorometanosulfonato de 2,2,2-trifluoroetilo
Purity:
≥ 98% (GC)
Synonym(s):
Éster 2,2,2-trifluoroetílico del ácido trifluorometanosulfónico, Triflato de 2,2,2-trifluoroetilo
Hazmat
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Product Information

2,2,2-Trifluoroethyl trifluoromethanesulfonate is a highly versatile reagent widely utilized in organic synthesis and pharmaceutical development. This compound is recognized for its exceptional ability to introduce trifluoromethyl groups into organic molecules, making it invaluable in the creation of fluorinated compounds that exhibit enhanced biological activity and stability. Its unique trifluoromethanesulfonate moiety allows for efficient nucleophilic substitution reactions, facilitating the formation of complex structures that are crucial in drug discovery and agrochemical applications. Researchers appreciate its effectiveness in producing fluorinated intermediates, which are often key components in the synthesis of novel therapeutics and materials.

The compound's stability and reactivity profile make it an ideal choice for various applications, including the synthesis of fluorinated pharmaceuticals, agrochemicals, and advanced materials. Its ability to enhance the lipophilicity and metabolic stability of drug candidates positions it as a preferred reagent in medicinal chemistry. Additionally, 2,2,2-Trifluoroethyl trifluoromethanesulfonate stands out for its ease of handling and compatibility with a range of reaction conditions, making it a reliable option for both academic and industrial laboratories.

Synonyms
Éster 2,2,2-trifluoroetílico del ácido trifluorometanosulfónico, Triflato de 2,2,2-trifluoroetilo
CAS Number
6226-25-1
Purity
≥ 98% (GC)
Molecular Formula
C3H2F6O3S
Molecular Weight
232.1
MDL Number
MFCD00671579
PubChem ID
80366
Density
1.61
Appearance
Líquido transparente, incoloro a amarillo.
Boiling Point
91 °C (Literatura)
Refractive Index
número 20/D 1.31
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Éster 2,2,2-trifluoroetílico del ácido trifluorometanosulfónico, Triflato de 2,2,2-trifluoroetilo
CAS Number
6226-25-1
Purity
≥ 98% (GC)
Molecular Formula
C3H2F6O3S
Molecular Weight
232.1
MDL Number
MFCD00671579
PubChem ID
80366
Density
1.61
Appearance
Líquido transparente, incoloro a amarillo.
Boiling Point
91 °C (Literatura)
Refractive Index
número 20/D 1.31
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,2,2-Trifluoroethyl trifluoromethanesulfonate is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a valuable reagent in organic synthesis, particularly for introducing trifluoromethyl groups into various organic molecules, enhancing their stability and reactivity.
  • Pharmaceutical Development: It plays a crucial role in the design of novel pharmaceuticals, especially in creating compounds with improved bioavailability and therapeutic efficacy due to the unique properties imparted by the trifluoroethyl group.
  • Material Science: Used in the development of advanced materials, it contributes to the creation of fluorinated polymers and coatings, which exhibit superior chemical resistance and thermal stability.
  • Environmental Research: The compound is important in studies related to greenhouse gas emissions, helping researchers understand the behavior of fluorinated compounds in the atmosphere and their environmental impact.
  • Analytical Chemistry: It is utilized as a derivatizing agent in analytical methods, improving the detection and quantification of various analytes in complex mixtures, thus enhancing the accuracy of chemical analyses.

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