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Atomfair Hexanoic acid, 2,2,2-trifluoroethyl ester C8H13F3O2
Description Hexanoic acid, 2,2,2-trifluoroethyl ester (CAS No. 2822-57-3) is a high-purity fluorinated ester compound with the molecular formula C8H13F3O2. This specialty chemical, also known by its IUPAC name 2,2,2-trifluoroethyl hexanoate , is widely utilized in advanced research and industrial applications due to its unique fluorinated structure. The compound exhibits excellent solvent properties and chemical stability, making it suitable for use in organic synthesis, material science, and pharmaceutical intermediates. Our product is rigorously tested for purity and consistency, ensuring optimal performance in demanding laboratory and production environments. Available in various quantities to meet your research needs.
Description
Description
Hexanoic acid, 2,2,2-trifluoroethyl ester (CAS No. 2822-57-3) is a high-purity fluorinated ester compound with the molecular formula C8H13F3O2. This specialty chemical, also known by its IUPAC name 2,2,2-trifluoroethyl hexanoate, is widely utilized in advanced research and industrial applications due to its unique fluorinated structure. The compound exhibits excellent solvent properties and chemical stability, making it suitable for use in organic synthesis, material science, and pharmaceutical intermediates. Our product is rigorously tested for purity and consistency, ensuring optimal performance in demanding laboratory and production environments. Available in various quantities to meet your research needs.
- CAS No: 2822-57-3
- Molecular Formula: C8H13F3O2
- Molecular Weight: 198.18
- Exact Mass: 198.08676414
- Monoisotopic Mass: 198.08676414
- IUPAC Name: 2,2,2-trifluoroethyl hexanoate
- SMILES: CCCCCC(=O)OCC(F)(F)F
- Synonyms: Hexanoic acid, 2,2,2-trifluoroethyl ester, SCHEMBL2692664, 2,2,2-Trifluoroethyl?Hexanoate, 2822-57-3
Application
Hexanoic acid, 2,2,2-trifluoroethyl ester is commonly employed as a fluorinated solvent or intermediate in organic synthesis, particularly in the preparation of specialty polymers and agrochemicals. Its unique trifluoroethyl group enhances reactivity in esterification and transesterification reactions. Researchers also utilize this compound in the development of novel materials with tailored surface properties due to its hydrophobic and oleophobic characteristics. Additionally, it serves as a key building block in pharmaceutical research for the synthesis of fluorinated active ingredients.
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