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Atomfair 3,5-Difluoro-2-methoxybenzaldehyde C8H6F2O2
Description 3,5-Difluoro-2-methoxybenzaldehyde (CAS No. 63954-77-8) is a high-purity fluorinated aromatic aldehyde with the molecular formula C8H6F2O2. This compound is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both fluorine and methoxy substituents, enhances reactivity and selectivity in cross-coupling reactions, nucleophilic additions, and other key transformations. Suitable for researchers and scientists, our product is rigorously tested for quality, ensuring optimal performance in your applications. Available in various quantities with detailed technical data, including NMR, HPLC, and MS spectra, to support your research needs.
Description
Description
3,5-Difluoro-2-methoxybenzaldehyde (CAS No. 63954-77-8) is a high-purity fluorinated aromatic aldehyde with the molecular formula C8H6F2O2. This compound is a versatile building block in organic synthesis, particularly in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique structure, featuring both fluorine and methoxy substituents, enhances reactivity and selectivity in cross-coupling reactions, nucleophilic additions, and other key transformations. Suitable for researchers and scientists, our product is rigorously tested for quality, ensuring optimal performance in your applications. Available in various quantities with detailed technical data, including NMR, HPLC, and MS spectra, to support your research needs.
- CAS No: 63954-77-8
- Molecular Formula: C8H6F2O2
- Molecular Weight: 172.13
- Exact Mass: 172.03358575
- Monoisotopic Mass: 172.03358575
- IUPAC Name: 3,5-difluoro-2-methoxybenzaldehyde
- SMILES: COC1=C(C=C(C=C1F)F)C=O
- Synonyms: 3,5-Difluoro-2-methoxybenzaldehyde, 131782-50-8, Benzaldehyde, 3,5-difluoro-2-methoxy-, 3,5-difluoro-2-methoxy-benzaldehyde, C8H6F2O2
Application
3,5-Difluoro-2-methoxybenzaldehyde is widely used as an intermediate in the synthesis of bioactive molecules, including pharmaceuticals and agrochemicals. Its electron-withdrawing fluorine atoms and electron-donating methoxy group make it valuable in designing compounds with tailored electronic properties. Researchers utilize this aldehyde in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions to construct complex aromatic systems. It is also employed in the development of liquid crystals and advanced polymeric materials due to its structural versatility.
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