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Catalog Number:
46463
CAS Number:
179260-78-7
4-méthyl-2-pyridyle trifluorométhanesulfonate
Purity:
≥ 97% (CG)
Synonym(s):
Ester 4-méthyl-2-pyridylique de l'acide trifluorométhanesulfonique
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Product Information

4-Methyl-2-pyridyl trifluoromethanesulfonate is a versatile chemical compound known for its unique trifluoromethanesulfonate group, which enhances its reactivity and utility in various applications. This compound serves as an effective electrophilic reagent in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its ability to act as a leaving group makes it invaluable in nucleophilic substitution reactions, allowing researchers and industry professionals to streamline complex synthetic pathways.

Additionally, 4-Methyl-2-pyridyl trifluoromethanesulfonate is utilized in the development of pharmaceuticals and agrochemicals, where it plays a crucial role in the modification of biologically active compounds. Its stability and compatibility with various reaction conditions make it a preferred choice for chemists looking to optimize their synthetic routes. With its distinct properties and practical applications, this compound stands out as a key reagent for advancing research and innovation in chemical synthesis.

Synonyms
Ester 4-méthyl-2-pyridylique de l'acide trifluorométhanesulfonique
CAS Number
179260-78-7
Purity
≥ 97% (CG)
Molecular Formula
C 7 H 6 F 3 NON 3 S
Molecular Weight
241.18
MDL Number
MFCD11042681
PubChem ID
10857619
Density
1.42
Appearance
Liquide transparent incolore à jaune clair à orange clair
Refractive Index
n20D 1.44
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Ester 4-méthyl-2-pyridylique de l'acide trifluorométhanesulfonique
CAS Number
179260-78-7
Purity
≥ 97% (CG)
Molecular Formula
C 7 H 6 F 3 NON 3 S
Molecular Weight
241.18
MDL Number
MFCD11042681
PubChem ID
10857619
Density
1.42
Appearance
Liquide transparent incolore à jaune clair à orange clair
Refractive Index
n20D 1.44
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4-Methyl-2-pyridyl trifluoromethanesulfonate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as an effective reagent for the synthesis of various organic compounds, particularly in the formation of carbon-carbon bonds, making it valuable for chemists in developing new materials.
  • Pharmaceutical Development: It plays a crucial role in the pharmaceutical industry by facilitating the synthesis of biologically active molecules, aiding researchers in drug discovery and development processes.
  • Catalysis: The compound is employed as a catalyst in several chemical reactions, enhancing reaction rates and selectivity, which is essential for efficient production in chemical manufacturing.
  • Fluorination Reactions: Its unique trifluoromethanesulfonate group allows for selective fluorination of substrates, which is important in producing fluorinated compounds used in agrochemicals and pharmaceuticals.
  • Material Science: This chemical is utilized in the development of advanced materials, including polymers and coatings, due to its ability to modify surface properties and enhance material performance.

Citations