Description

1-Bromo-1,1,2,2-tetrafluoro-3-octene (CAS: 74793-72-9) is a high-purity fluorinated organic compound with the molecular formula C₈H₁₁BrF₄. This specialty chemical is designed for advanced research applications, particularly in organic synthesis, material science, and pharmaceutical development. Its unique bromo- and tetrafluoro-substituted alkene structure makes it a valuable intermediate for cross-coupling reactions, polymer modifications, and the synthesis of fluorinated derivatives. Available in various quantities with >98% purity (GC), this product is rigorously tested for consistency and stability, ensuring reliable performance in sensitive experiments. Suitable for use in academic, industrial, and government laboratories, it is supplied with comprehensive analytical data (NMR, MS, HPLC) and stored under optimal conditions to maintain integrity.

Properties

• CAS Number: 74793-72-9
• Complexity: 177
• IUPAC Name: (E)-1-bromo-1,1,2,2-tetrafluoro-oct-3-ene
• InChI: InChI=1S/C8H11BrF4/c1-2-3-4-5-6-7(10,11)8(9,12)13/h5-6H,2-4H2,1H3/b6-5+
• InChI Key: ZIUUSJGUQRYFKK-AATRIKPKSA-N
• Exact Mass: 261.99803
• Molecular Formula: C8H11BrF4
• Molecular Weight: 263.07
• SMILES: CCCC/C=C/C(C(F)(F)Br)(F)F
• Monoisotopic Mass: 261.99803
• Synonyms: 1-Bromo-1,1,2,2-tetrafluoro-3-octene, 74793-72-9, DTXSID50418611, DTXCID70369459, 1-bromo-1,1,2,2-tetrafluorooct-3-ene, (E)-1-bromo-1,1,2,2-tetrafluorooct-3-ene, 3-Octene, 1-bromo-1,1,2,2-tetrafluoro-, MFCD00153715, 3-Octene,1-bromo-1,1,2,2-tetrafluoro-, (3E)-1-bromo-1,1,2,2-tetrafluorooct-3-ene, ZIUUSJGUQRYFKK-AATRIKPKSA-N, SBB102621, AKOS015833888, (E)-1-bromo-1,1,2,2-tetrafluoro-3-octene, (3E)-1-Bromo-1,1,2,2-tetrafluoro-3-octene #, A838230, (E)-1-bromanyl-1,1,2,2-tetrakis(fluoranyl)oct-3-ene

1-Bromo-1,1,2,2-tetrafluoro-3-octene serves as a key building block in the synthesis of fluorinated polymers and agrochemicals due to its reactive alkene and halogen functionalities. Researchers utilize it in palladium-catalyzed cross-coupling reactions to introduce tetrafluoroalkyl groups into complex molecules. Its stability under acidic conditions makes it suitable for developing corrosion-resistant coatings. In pharmaceuticals, it is explored as a precursor for bioactive compounds with enhanced metabolic stability.

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