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Atomfair 4′-Bromo-3′-fluoroacetanilide C8H7BrFNO
Description 4′-Bromo-3′-fluoroacetanilide (CAS No. 351-30-4) is a high-purity bromo- and fluoro-substituted acetanilide derivative with the molecular formula C8H7BrFNO . This compound, also known as N-(4-bromo-3-fluorophenyl)acetamide , is a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure, featuring both bromo and fluoro substituents on the aromatic ring, makes it a versatile building block for the development of novel bioactive molecules, agrochemicals, and materials. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder. Suitable for use in cross-coupling reactions, medicinal chemistry, and as a precursor for further functionalization.…
Description
Description
4′-Bromo-3′-fluoroacetanilide (CAS No. 351-30-4) is a high-purity bromo- and fluoro-substituted acetanilide derivative with the molecular formula C8H7BrFNO. This compound, also known as N-(4-bromo-3-fluorophenyl)acetamide, is a valuable intermediate in organic synthesis and pharmaceutical research. Its unique structure, featuring both bromo and fluoro substituents on the aromatic ring, makes it a versatile building block for the development of novel bioactive molecules, agrochemicals, and materials. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder. Suitable for use in cross-coupling reactions, medicinal chemistry, and as a precursor for further functionalization. Packaged under inert gas to ensure stability and longevity.
- CAS No: 351-30-4
- Molecular Formula: C8H7BrFNO
- Molecular Weight: 232.05
- Exact Mass: 230.96950
- Monoisotopic Mass: 230.96950
- IUPAC Name: N-(4-bromo-3-fluorophenyl)acetamide
- SMILES: CC(=O)NC1=CC(=C(C=C1)Br)F
- Synonyms: 351-30-4, 4′-Bromo-3′-fluoroacetanilide, N-(4-bromo-3-fluorophenyl)acetamide, DTXSID90378366, DTXCID90329393
Application
4′-Bromo-3′-fluoroacetanilide is widely utilized as a key intermediate in pharmaceutical research, particularly in the synthesis of fluorinated drug candidates. Its bromo and fluoro substituents enable participation in palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings. Researchers also employ this compound in the development of agrochemicals and specialty materials due to its robust aromatic framework. Its acetamide moiety serves as a protective group or functional handle for further derivatization.
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