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Atomfair Trifluoroacetamide C2H2F3NO
Description Trifluoroacetamide (CAS No. 354-38-1) is a high-purity fluorinated organic compound with the molecular formula C2H2F3NO and IUPAC name 2,2,2-trifluoroacetamide . This specialized reagent is widely utilized in synthetic chemistry, pharmaceutical research, and material science due to its unique trifluoromethyl group, which enhances reactivity and stability in various reactions. Our product is rigorously tested to ensure ??98% purity (GC), making it ideal for precise applications such as peptide synthesis, derivatization, and as a precursor for fluorinated compounds. Packaged under inert conditions to maintain integrity, Trifluoroacetamide is available in quantities ranging from grams to kilograms, with custom packaging options available upon…
Description
Description
Trifluoroacetamide (CAS No. 354-38-1) is a high-purity fluorinated organic compound with the molecular formula C2H2F3NO and IUPAC name 2,2,2-trifluoroacetamide. This specialized reagent is widely utilized in synthetic chemistry, pharmaceutical research, and material science due to its unique trifluoromethyl group, which enhances reactivity and stability in various reactions. Our product is rigorously tested to ensure ??98% purity (GC), making it ideal for precise applications such as peptide synthesis, derivatization, and as a precursor for fluorinated compounds. Packaged under inert conditions to maintain integrity, Trifluoroacetamide is available in quantities ranging from grams to kilograms, with custom packaging options available upon request. Suitable for use in HPLC, NMR, and other analytical techniques.
- CAS No: 354-38-1
- Molecular Formula: C2H2F3NO
- Molecular Weight: 113.04
- Exact Mass: 113.00884817
- Monoisotopic Mass: 113.00884817
- IUPAC Name: 2,2,2-trifluoroacetamide
- SMILES: C(=O)(C(F)(F)F)N
- Synonyms: Trifluoroacetamide, 2,2,2-Trifluoroacetamide, Acetamide, 2,2,2-trifluoro-, UNII-36MU16BYFK, 2,2,2-Trifluoro-acetamide
Application
Trifluoroacetamide is commonly employed as a versatile building block in organic synthesis, particularly in the preparation of fluorinated pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of trifluoroacetyl-protected amines and peptides, enhancing stability during complex reactions. Researchers also utilize it in derivatization protocols for GC-MS analysis due to its excellent volatility and detection sensitivity. Additionally, its electron-withdrawing properties make it valuable in material science for modifying polymer properties.
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