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Catalog Number:
48048
CAS Number:
361447-81-6
Trifluorométhanesulfonate de 1-phényl-1 H -imidazol-3-ium
Purity:
≥ 98 % (HPLC)
Synonym(s):
Triflate de 1-phényl-1 H -imidazol-3-ium
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Product Information

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Synonyms
Triflate de 1-phényl-1 H -imidazol-3-ium
CAS Number
361447-81-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H9F3N2O3S
Molecular Weight
294.25
MDL Number
MFCD32632561
Melting Point
126 - 131 °C
Appearance
Poudre blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Triflate de 1-phényl-1 H -imidazol-3-ium
CAS Number
361447-81-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C10H9F3N2O3S
Molecular Weight
294.25
MDL Number
MFCD32632561
Melting Point
126 - 131 °C
Appearance
Poudre blanche à jaune clair
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1-Phenyl-1H-imidazol-3-ium trifluoromethanesulfonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic synthesis, facilitating the formation of various carbon-carbon and carbon-heteroatom bonds, which is essential for creating complex molecules in pharmaceuticals.
  • Catalysis: It acts as a catalyst in numerous chemical reactions, enhancing reaction rates and selectivity, particularly in the synthesis of heterocycles, which are crucial in drug development.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, where its unique properties can improve durability and performance.
  • Biochemistry: It plays a role in biochemical assays and studies, aiding researchers in understanding enzyme mechanisms and interactions, which is vital for drug discovery.
  • Electrochemistry: This chemical is employed in electrochemical applications, such as sensors and batteries, where it contributes to improved efficiency and stability of the devices.

Citations