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Atomfair 2,5-Difluorotoluene C7H6F2
Description 2,5-Difluorotoluene (CAS No. 452-67-5) is a high-purity fluorinated aromatic compound with the molecular formula C7H6F2and IUPAC name 1,4-difluoro-2-methylbenzene . This specialty chemical is rigorously synthesized and purified to meet the stringent requirements of pharmaceutical, agrochemical, and materials science research. With its stable benzene ring substituted by two fluorine atoms at the 1 and 4 positions and a methyl group at the 2 position, it serves as a versatile building block for advanced organic synthesis. Available in sealed amber vials under inert atmosphere to ensure stability, our product is characterized by GC-MS, NMR, and elemental analysis with ??98% purity. Ideal…
Description
Description
2,5-Difluorotoluene (CAS No. 452-67-5) is a high-purity fluorinated aromatic compound with the molecular formula C7H6F2 and IUPAC name 1,4-difluoro-2-methylbenzene. This specialty chemical is rigorously synthesized and purified to meet the stringent requirements of pharmaceutical, agrochemical, and materials science research. With its stable benzene ring substituted by two fluorine atoms at the 1 and 4 positions and a methyl group at the 2 position, it serves as a versatile building block for advanced organic synthesis. Available in sealed amber vials under inert atmosphere to ensure stability, our product is characterized by GC-MS, NMR, and elemental analysis with ??98% purity. Ideal for nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor for liquid crystal materials.
- CAS No: 452-67-5
- Molecular Formula: C7H6F2
- Molecular Weight: 128.12
- Exact Mass: 128.04375652
- Monoisotopic Mass: 128.04375652
- IUPAC Name: 1,4-difluoro-2-methylbenzene
- SMILES: CC1=C(C=CC(=C1)F)F
- Synonyms: 2,5-Difluorotoluene, 1,4-Difluoro-2-methylbenzene, Benzene, 1,4-difluoro-2-methyl-, 7K9PUS3HC7, EINECS 207-205-6
Application
2,5-Difluorotoluene is widely employed as a key intermediate in pharmaceutical development, particularly for modifying drug bioavailability through fluorination strategies. Its electron-deficient aromatic ring facilitates palladium-catalyzed coupling reactions in agrochemical synthesis. Researchers also utilize this compound in materials science for designing fluorinated polymers with enhanced thermal stability. The methyl group offers additional functionalization sites for tailored molecular architectures.
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