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Atomfair 1,3-Bis(1,1,2,2-tetrafluoroethoxy)benzene C10H6F8O2
Description 1,3-Bis(1,1,2,2-tetrafluoroethoxy)benzene (CAS No. 3914-19-0) is a high-purity fluorinated aromatic compound with the molecular formula C10H6F8O2. This specialty chemical features a benzene core symmetrically substituted with two 1,1,2,2-tetrafluoroethoxy groups, offering unique physicochemical properties such as enhanced thermal stability, chemical resistance, and low surface energy. Ideal for advanced research applications, this compound is meticulously synthesized and purified to meet stringent quality standards, ensuring optimal performance in demanding environments. Available in various quantities, it is supplied with comprehensive analytical documentation including1H NMR,19F NMR, GC/MS, and HPLC data for verification.
Description
Description
1,3-Bis(1,1,2,2-tetrafluoroethoxy)benzene (CAS No. 3914-19-0) is a high-purity fluorinated aromatic compound with the molecular formula C10H6F8O2. This specialty chemical features a benzene core symmetrically substituted with two 1,1,2,2-tetrafluoroethoxy groups, offering unique physicochemical properties such as enhanced thermal stability, chemical resistance, and low surface energy. Ideal for advanced research applications, this compound is meticulously synthesized and purified to meet stringent quality standards, ensuring optimal performance in demanding environments. Available in various quantities, it is supplied with comprehensive analytical documentation including 1H NMR, 19F NMR, GC/MS, and HPLC data for verification.
- CAS No: 3914-19-0
- Molecular Formula: C10H6F8O2
- Molecular Weight: 310.14
- Exact Mass: 310.02400473
- Monoisotopic Mass: 310.02400473
- IUPAC Name: 1,3-bis(1,1,2,2-tetrafluoroethoxy)benzene
- SMILES: C1=CC(=CC(=C1)OC(C(F)F)(F)F)OC(C(F)F)(F)F
- Synonyms: 1,3-Bis(1,1,2,2-tetrafluoroethoxy)benzene, Benzene, 1,3-bis(1,1,2,2-tetrafluoroethoxy)-, EINECS 223-476-3, DTXSID0063232, DTXCID2039598
Application
1,3-Bis(1,1,2,2-tetrafluoroethoxy)benzene is primarily utilized as a building block in the synthesis of fluorinated polymers and liquid crystals, where its rigid aromatic core and fluorinated side chains contribute to exceptional thermal and chemical stability. It serves as a key intermediate in the development of high-performance lubricants, coatings, and dielectric materials for aerospace and electronics industries. Researchers also employ this compound in supramolecular chemistry and catalysis studies due to its electron-withdrawing properties and steric effects.
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