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Trifluoroacetamide CAS: 354-38-1

Short Description:

Catalog Number: XD93505
Cas: 354-38-1
Molecular Formula: C2H2F3NO
Molecular Weight: 113.04
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Product Detail

Product Tags

Catalog Number XD93505
Product Name Trifluoroacetamide
CAS 354-38-1
Molecular Formula C2H2F3NO
Molecular Weight 113.04
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

Trifluoroacetamide, with the chemical formula CF3CONH2, is a compound that finds various applications in different fields, including pharmaceutical, agrochemical, and industrial sectors.In the pharmaceutical industry, trifluoroacetamide plays a significant role as a protecting group in organic synthesis. Protecting groups are functional groups temporarily attached to specific atoms in a molecule to prevent unwanted reactions during chemical transformations. Trifluoroacetamide acts as a protecting group for amines, particularly primary amines. By derivatizing a primary amine with trifluoroacetamide, it effectively prevents unwanted side reactions, allowing selective modification of other functional groups present in the molecule. This protection-deprotection strategy is widely used in the synthesis of complex pharmaceutical compounds, ensuring specific chemical reactions occur only at predetermined sites.Moreover, trifluoroacetamide is employed in the production of Vilsmeier-Haack reagents. Vilsmeier-Haack reaction is a chemical reaction used for the synthesis of various organic compounds, including aromatic aldehydes and ketones. Trifluoroacetamide, in combination with an acid chloride and a Lewis acid catalyst, forms the Vilsmeier-Haack reagent, which acts as a versatile tool for the functionalization of aromatic compounds. This reaction is widely utilized in the pharmaceutical industry for the synthesis of intermediates and active pharmaceutical ingredients (APIs).In the agrochemical sector, trifluoroacetamide is utilized as an intermediate in the synthesis of herbicides and pesticides. The compound's reactive nature allows for the introduction of specific functional groups required for agrochemical activity. Trifluoroacetamide-based molecules can display improved herbicidal or pesticidal properties compared to their analogs, enhancing their efficacy in protecting crops against weeds, pests, and diseases. Trifluoroacetamide derivatives have demonstrated potent activity against a broad spectrum of target organisms while minimizing their adverse impact on the environment.Furthermore, trifluoroacetamide has applications in the industrial sector. It is involved in the production of solvents, such as N-methyl-N-(trifluoroacetyl)acetamide (MTAA), used in various industrial processes. Trifluoroacetamide-containing solvents have desirable properties, including high boiling points, low vapor pressures, and chemical stability, making them suitable for applications such as extraction, separation, and purification of organic compounds.In summary, trifluoroacetamide plays a crucial role in organic synthesis, particularly in pharmaceutical and agrochemical applications. It serves as a protecting group for amines, allowing selective modifications during complex organic synthesis. Trifluoroacetamide-based compounds find use as intermediates in the production of pharmaceuticals, herbicides, and pesticides, providing improved efficacy and environmental sustainability. Additionally, trifluoroacetamide is involved in the production of specialized solvents used in various industrial processes. The versatility and reactivity of trifluoroacetamide make it a valuable compound in multiple industries.


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    Trifluoroacetamide CAS: 354-38-1