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2-amino-N-(2,2,2-trifluoroethyl)acetamide(HCL) CAS: 1171331-39-7

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Catalog Number: XD93379
Cas: 1171331-39-7
Molecular Formula: C4H8ClF3N2O
Molecular Weight: 192.57
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Product Detail

Product Tags

Catalog Number XD93379
Product Name 2-amino-N-(2,2,2-trifluoroethyl)acetamide(HCL)
CAS 1171331-39-7
Molecular Formula C4H8ClF3N2O
Molecular Weight 192.57
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride, often referred to as TFAA hydrochloride, is a chemical compound with the molecular formula C5H10ClF3N2O. This compound finds application in several industries due to its unique properties and versatile nature.One of the primary uses of 2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride is in the synthesis of pharmaceutical compounds. It serves as a valuable intermediate in the production of various drugs and active pharmaceutical ingredients (APIs). The amino group and the acetamide functional group present in this compound make it an essential building block in the synthesis of complex organic molecules. TFAA hydrochloride's reactivity and compatibility with a wide range of chemical reactions make it highly versatile for pharmaceutical synthesis, enabling the development of novel drugs and therapeutic agents.Moreover, 2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride is utilized in the field of analytical chemistry as a derivatizing agent. It can react with various compounds to form stable derivatives that are amenable to analysis using techniques like gas chromatography (GC) or liquid chromatography (LC). This compound finds particular importance in the analysis of amino acids and other amine-containing compounds, where it helps enhance their detectability, separation, and quantification.Furthermore, 2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride is employed in the field of organic synthesis as a useful reagent. Its trifluoroethyl group, known for its electron-withdrawing properties, can be leveraged to introduce fluorine atoms into organic molecules, leading to the synthesis of fluorinated compounds. Fluorinated organic compounds often possess unique properties such as improved stability, altered reactivity, and enhanced pharmacological activity. TFAA hydrochloride's ability to introduce fluorine atoms in organic synthesis makes it an important tool in medicinal chemistry, agrochemicals, and materials science.Additionally, 2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride is utilized in the field of polymer science as a crosslinking agent or modifier. By incorporating this compound into polymer formulations, the physical and chemical properties of polymers can be altered, leading to improved performance characteristics. TFAA hydrochloride can contribute to the development of new polymer materials with enhanced mechanical strength, thermal stability, and resistance to degradation.In summary, 2-amino-N-(2,2,2-trifluoroethyl)acetamide hydrochloride, or TFAA hydrochloride, finds important applications in pharmaceutical synthesis, analytical chemistry, organic synthesis, and polymer science. Its unique properties, including the amino and trifluoroethyl groups, make it valuable as an intermediate for drug synthesis, a derivatizing agent for analytical purposes, a fluorinating reagent for organic synthesis, and a modifier in polymer formulations. Its versatility and compatibility with diverse chemical processes continue to drive research and innovation in various industries.


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    2-amino-N-(2,2,2-trifluoroethyl)acetamide(HCL) CAS: 1171331-39-7