Description

1-(4-Bromo-2-fluorophenyl)ethan-1-one (CAS: 625446-22-2) is a high-purity organic compound with the molecular formula C₈H₆BrFO, widely used as a key intermediate in pharmaceutical synthesis and material science research. This aromatic ketone features a bromo-fluorophenyl backbone, making it valuable for cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig aminations. Our product is rigorously tested for purity (>98% by HPLC) and is supplied in sealed, light-resistant packaging to ensure stability. Ideal for researchers developing novel drug candidates, agrochemicals, or specialty polymers, this compound is handled under strict quality control (QC) protocols to meet industry standards. Available in gram to kilogram quantities with customizable packaging options.

Properties

• CAS Number: 625446-22-2
• Complexity: 160
• IUPAC Name: 1-(4-bromo-2-fluoro-phenyl)ethanone
• InChI: InChI=1S/C8H6BrFO/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4H,1H3
• InChI Key: ASKFCSCYGAFWAB-UHFFFAOYSA-N
• Exact Mass: 215.95861
• Molecular Formula: C8H6BrFO
• Molecular Weight: 217.03
• SMILES: CC(=O)C1=C(C=C(C=C1)Br)F
• Topological: 17.1
• Monoisotopic Mass: 215.95861
• Synonyms: 625446-22-2, 1-(4-bromo-2-fluorophenyl)ethan-1-one, DTXSID30620396, DTXCID10571150, 814-022-0, 4-Bromo-2-fluoroacetophenone, 1-(4-Bromo-2-fluorophenyl)ethanone, 4′-BROMO-2′-FLUOROACETOPHENONE, 1-Acetyl-4-bromo-2-fluorobenzene, 1-(4-Bromo-2-fluoro-phenyl)-ethanone, MFCD03411551, Ethanone, 1-(4-bromo-2-fluorophenyl)-, SCHEMBL8204, SCHEMBL2095201, 4-fluoroacetophenone, CHEMBL5277466, SCHEMBL26613950, ASKFCSCYGAFWAB-UHFFFAOYSA-N, CL8664, SBB095352, 1-(4-bromo-2-fluorophenyl)-ethanone, AKOS005259579, CS-W004323, FB64516, MB02747, PS-7922, AC-28596, SY024301, 1-(4-bromanyl-2-fluoranyl-phenyl)ethanone, B5236, EN300-111817, A833836, Z1269134115, 4 inverted exclamation mark -Bromo-2 inverted exclamation mark -fluoroacetophenone

1-(4-Bromo-2-fluorophenyl)ethan-1-one serves as a versatile building block in medicinal chemistry, particularly for synthesizing fluorinated bioactive molecules. It is employed in palladium-catalyzed coupling reactions to create complex aryl structures for drug discovery. Researchers also utilize it in the development of liquid crystal materials and organic semiconductors due to its electron-withdrawing properties. Suitable for lab-scale experiments and industrial R&D under controlled conditions.

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