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Catalog Number:
00290
CAS Number:
354-38-1
Trifluoroacétamide
Purity:
≥ 99 % (dosage)
Synonym(s):
Amide d'acide trifluoroacétique, 2,2,2-Trifluoroacétamide
Documents
$18.53 /25G
Taille
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Informations sur le produit

2,2,2-Trifluoroacetamide is a versatile compound widely recognized for its unique properties and applications in various fields, including pharmaceuticals, agrochemicals, and material science. This fluorinated amide exhibits excellent thermal stability and solubility in organic solvents, making it an ideal candidate for use as a reagent in organic synthesis. Its trifluoromethyl group enhances its reactivity, allowing it to participate in a range of chemical reactions, such as nucleophilic substitutions and condensation reactions. Researchers often utilize 2,2,2-Trifluoroacetamide in the synthesis of fluorinated compounds, which are crucial in developing new drugs and agrochemicals with improved efficacy and reduced environmental impact.

In addition to its synthetic applications, 2,2,2-Trifluoroacetamide is also employed in analytical chemistry as a derivatizing agent for the analysis of various functional groups. Its ability to form stable derivatives aids in the detection and quantification of target compounds, making it invaluable in laboratories focused on environmental monitoring and quality control. With its unique properties and diverse applications, 2,2,2-Trifluoroacetamide stands out as a key compound for researchers and industry professionals seeking innovative solutions in chemical synthesis and analysis.

Numéro CAS 
354-38-1
Formule moléculaire
C 2 H 2 F 3 NON
Poids moléculaire 
113.04
Point de fusion 
65-70 °C
Informations générales
Numéro CAS 
354-38-1
Formule moléculaire
C 2 H 2 F 3 NON
Poids moléculaire 
113.04
Point de fusion 
65-70 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
-
Applications

2,2,2-Trifluoroacetamide is widely utilized in research focused on:

  • Organic Synthesis: It serves as a versatile reagent in the synthesis of various organic compounds, particularly in the preparation of fluorinated amides, which are valuable in pharmaceuticals.
  • Analytical Chemistry: This compound is used as a derivatizing agent for the analysis of amino acids and other polar compounds, enhancing their detectability in chromatographic techniques.
  • Pharmaceutical Development: Its unique properties make it useful in drug formulation, especially in designing compounds with improved bioavailability and stability.
  • Material Science: It is employed in the development of fluorinated polymers, which exhibit excellent thermal and chemical resistance, making them suitable for high-performance applications.
  • Environmental Chemistry: The compound is utilized in studies related to the behavior of fluorinated compounds in the environment, aiding in the assessment of their impact and degradation pathways.

Citations