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Atomfair 3,5-Difluorophenol C6H4F2O
Description 3,5-Difluorophenol (CAS No. 2713-34-0) is a fluorinated phenolic compound with the molecular formula C6H4F2O . This high-purity reagent is widely used in organic synthesis, pharmaceutical research, and material science due to its unique structural properties. The presence of two fluorine atoms at the meta positions of the phenol ring enhances its reactivity and selectivity in nucleophilic aromatic substitution reactions, making it a valuable intermediate for the development of advanced chemicals and bioactive molecules. Our 3,5-Difluorophenol is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers to maintain stability and prevent degradation. Suitable for use in…
Description
Description
3,5-Difluorophenol (CAS No. 2713-34-0) is a fluorinated phenolic compound with the molecular formula C6H4F2O. This high-purity reagent is widely used in organic synthesis, pharmaceutical research, and material science due to its unique structural properties. The presence of two fluorine atoms at the meta positions of the phenol ring enhances its reactivity and selectivity in nucleophilic aromatic substitution reactions, making it a valuable intermediate for the development of advanced chemicals and bioactive molecules.
Our 3,5-Difluorophenol is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed containers to maintain stability and prevent degradation. Suitable for use in HPLC, LC-MS, and NMR applications, this compound is an essential building block for researchers working on fluorinated aromatic systems, agrochemicals, and pharmaceutical candidates.
- CAS No: 2713-34-0
- Molecular Formula: C6H4F2O
- Molecular Weight: 130.09
- Exact Mass: 130.02302107
- Monoisotopic Mass: 130.02302107
- IUPAC Name: 3,5-difluorophenol
- SMILES: C1=C(C=C(C=C1F)F)O
- Synonyms: 3,5-Difluorophenol, 2713-34-0, Phenol, 3,5-difluoro-, Phenol,3,5-difluoro-, HJSSBIMVTMYKPD-UHFFFAOYSA-
Application
3,5-Difluorophenol serves as a key intermediate in the synthesis of fluorinated pharmaceuticals, agrochemicals, and specialty materials. Its reactivity enables the preparation of complex molecules through Suzuki coupling, etherification, and other aromatic substitution reactions. Researchers also utilize this compound in the development of liquid crystals and polymer additives due to its electron-withdrawing properties.
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