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Atomfair 3-Fluoro-N-methoxy-N-methylbenzamide C9H10FNO2

Description 3-Fluoro-N-methoxy-N-methylbenzamide (CAS No. 226260-01-1) is a high-purity fluorinated benzamide derivative with the molecular formula C9H10FNO2. This compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique structural properties. The presence of both fluorine and methoxy-N-methylamide moieties enhances its reactivity, making it a valuable intermediate for constructing complex molecules. It is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for research applications. Proper storage under inert conditions at 2-8??C is recommended to maintain stability.

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Description

Description

3-Fluoro-N-methoxy-N-methylbenzamide (CAS No. 226260-01-1) is a high-purity fluorinated benzamide derivative with the molecular formula C9H10FNO2. This compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its unique structural properties. The presence of both fluorine and methoxy-N-methylamide moieties enhances its reactivity, making it a valuable intermediate for constructing complex molecules. It is supplied as a white to off-white crystalline powder with ??95% purity (HPLC), ensuring consistency for research applications. Proper storage under inert conditions at 2-8??C is recommended to maintain stability.

  • CAS No: 226260-01-1
  • Molecular Formula: C9H10FNO2
  • Molecular Weight: 183.18
  • Exact Mass: 183.06955672
  • Monoisotopic Mass: 183.06955672
  • IUPAC Name: 3-fluoro-N-methoxy-N-methylbenzamide
  • SMILES: CN(C(=O)C1=CC(=CC=C1)F)OC
  • Synonyms: 3-FLUORO-N-METHOXY-N-METHYLBENZAMIDE, 226260-01-1, MFCD02684305, SCHEMBL305837, DTXSID90611785

Application

3-Fluoro-N-methoxy-N-methylbenzamide serves as a versatile building block in medicinal chemistry for the synthesis of fluorinated drug candidates. Its electron-withdrawing fluorine group facilitates selective cross-coupling reactions, while the Weinreb amide functionality enables controlled carbonyl transformations. Researchers employ this compound in the development of kinase inhibitors and CNS-targeting molecules. It is also used in material science to modify polymer properties via incorporation of fluorinated aromatic units.

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