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Atomfair 2-Bromo-3-fluorophenol C6H4BrFO
Description 2-Bromo-3-fluorophenol (CAS No. 433939-27-6) is a high-purity halogenated phenol derivative with the molecular formula C6H4BrFO . This compound is characterized by the presence of both bromine and fluorine substituents on the aromatic phenol ring, making it a versatile intermediate for advanced organic synthesis and pharmaceutical research. Its IUPAC name, 2-bromo-3-fluorophenol , reflects its precise structural configuration. Suitable for use in cross-coupling reactions, nucleophilic substitutions, and as a building block for agrochemicals or bioactive molecules, this product is rigorously tested for purity and stability. Available in various quantities, it is ideal for researchers requiring reliable and consistent quality in their…
Description
Description
2-Bromo-3-fluorophenol (CAS No. 433939-27-6) is a high-purity halogenated phenol derivative with the molecular formula C6H4BrFO. This compound is characterized by the presence of both bromine and fluorine substituents on the aromatic phenol ring, making it a versatile intermediate for advanced organic synthesis and pharmaceutical research. Its IUPAC name, 2-bromo-3-fluorophenol, reflects its precise structural configuration. Suitable for use in cross-coupling reactions, nucleophilic substitutions, and as a building block for agrochemicals or bioactive molecules, this product is rigorously tested for purity and stability. Available in various quantities, it is ideal for researchers requiring reliable and consistent quality in their synthetic workflows.
- CAS No: 433939-27-6
- Molecular Formula: C6H4BrFO
- Molecular Weight: 191.00
- Exact Mass: 189.94296
- Monoisotopic Mass: 189.94296
- IUPAC Name: 2-bromo-3-fluorophenol
- SMILES: C1=CC(=C(C(=C1)F)Br)O
- Synonyms: 2-Bromo-3-fluorophenol, 443-81-2, DTXSID40479251, DTXCID60430061, 675-092-4
Application
2-Bromo-3-fluorophenol serves as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty materials. Its halogenated aromatic structure enables participation in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions. Researchers utilize this compound to develop fluorinated bioactive molecules or as a precursor for liquid crystal materials. It is also employed in the study of structure-activity relationships (SAR) in medicinal chemistry.
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