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Atomfair 4′-Fluoro-3′-nitroacetophenone C8H6FNO3
Description 4′-Fluoro-3′-nitroacetophenone (CAS 400-93-1) is a high-purity fluorinated nitroacetophenone derivative with the molecular formula C8H6FNO3. This compound, also known as 1-(4-fluoro-3-nitrophenyl)ethanone, is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both fluoro and nitro functional groups, makes it a valuable intermediate for the development of novel bioactive molecules. Our product is rigorously tested for purity and consistency, ensuring optimal performance in your laboratory applications. Available in various quantities to suit your research needs, this compound is handled and shipped with the utmost care to maintain its integrity.
Description
Description
4′-Fluoro-3′-nitroacetophenone (CAS 400-93-1) is a high-purity fluorinated nitroacetophenone derivative with the molecular formula C8H6FNO3. This compound, also known as 1-(4-fluoro-3-nitrophenyl)ethanone, is a versatile building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both fluoro and nitro functional groups, makes it a valuable intermediate for the development of novel bioactive molecules. Our product is rigorously tested for purity and consistency, ensuring optimal performance in your laboratory applications. Available in various quantities to suit your research needs, this compound is handled and shipped with the utmost care to maintain its integrity.
- CAS No: 400-93-1
- Molecular Formula: C8H6FNO3
- Molecular Weight: 183.14
- Exact Mass: 183.03317122
- Monoisotopic Mass: 183.03317122
- IUPAC Name: 1-(4-fluoro-3-nitrophenyl)ethanone
- SMILES: CC(=O)C1=CC(=C(C=C1)F)[N+](=O)[O-]
- Synonyms: 4′-Fluoro-3′-nitroacetophenone, 400-93-1, 1-(4-fluoro-3-nitrophenyl)ethanone, DTXSID60370392, DTXCID80321427
Application
4′-Fluoro-3′-nitroacetophenone is widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates. Its nitro group allows for further functionalization, making it valuable in the creation of complex organic molecules. Researchers also utilize this compound in material science for the development of specialty chemicals and advanced materials. Its fluorinated aromatic structure is particularly useful in studies involving electron-withdrawing groups and their effects on molecular properties.
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