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Atomfair Ethyl 4,4,4-trifluoro-2-butynoate C6H5F3O2

Description Ethyl 4,4,4-trifluoro-2-butynoate (CAS No. 79424-03-6) is a high-purity fluorinated alkyne ester with the molecular formula C6H5F3O2. This specialized chemical compound, also known by its IUPAC name ethyl 4,4,4-trifluorobut-2-ynoate , is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique trifluoromethyl group and reactive alkyne moiety. The product is rigorously tested for quality, ensuring optimal performance in advanced applications. Available in various quantities, it is packaged under inert conditions to maintain stability and purity. Ideal for researchers and scientists seeking precision reagents for fluorination reactions or building blocks for complex molecular architectures.

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Description

Description

Ethyl 4,4,4-trifluoro-2-butynoate (CAS No. 79424-03-6) is a high-purity fluorinated alkyne ester with the molecular formula C6H5F3O2. This specialized chemical compound, also known by its IUPAC name ethyl 4,4,4-trifluorobut-2-ynoate, is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique trifluoromethyl group and reactive alkyne moiety. The product is rigorously tested for quality, ensuring optimal performance in advanced applications. Available in various quantities, it is packaged under inert conditions to maintain stability and purity. Ideal for researchers and scientists seeking precision reagents for fluorination reactions or building blocks for complex molecular architectures.

  • CAS No: 79424-03-6
  • Molecular Formula: C6H5F3O2
  • Molecular Weight: 166.10
  • Exact Mass: 166.02416388
  • Monoisotopic Mass: 166.02416388
  • IUPAC Name: ethyl 4,4,4-trifluorobut-2-ynoate
  • SMILES: CCOC(=O)C#CC(F)(F)F
  • Synonyms: Ethyl 4,4,4-trifluoro-2-butynoate, 635-987-2, Ethyl 4,4,4-trifluorobut-2-ynoate, 79424-03-6, MFCD00192167

Application

Ethyl 4,4,4-trifluoro-2-butynoate serves as a versatile intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances metabolic stability and bioavailability in drug development. The compound is also employed in materials science for creating fluorinated polymers with unique properties. Researchers utilize it in click chemistry and cross-coupling reactions due to its reactive alkyne functionality.

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