Cas no 1803607-63-7 (2-fluoro-1-(methoxymethyl)-4-nitrobenzene)

2-Fluoro-1-(methoxymethyl)-4-nitrobenzene is a fluorinated aromatic compound featuring a methoxymethyl and nitro substituent on the benzene ring. Its unique structure makes it a valuable intermediate in organic synthesis, particularly for pharmaceuticals and agrochemicals. The presence of both electron-withdrawing (nitro) and electron-donating (methoxymethyl) groups enhances its reactivity in substitution and coupling reactions. The fluorine atom further contributes to its utility in designing bioactive molecules due to its influence on metabolic stability and binding affinity. This compound is characterized by high purity and stability, ensuring consistent performance in synthetic applications. Its versatility and well-defined chemical properties make it a preferred choice for researchers in medicinal and materials chemistry.
2-fluoro-1-(methoxymethyl)-4-nitrobenzene structure
1803607-63-7 structure
Product Name:2-fluoro-1-(methoxymethyl)-4-nitrobenzene
CAS No:1803607-63-7
MF:C8H8FNO3
MW:185.152425765991
CID:4617941
Update Time:2025-06-11

2-fluoro-1-(methoxymethyl)-4-nitrobenzene Chemical and Physical Properties

Names and Identifiers

    • 2-Fluoro-1-methoxymethyl-4-nitro-benzene
    • 2-fluoro-1-(methoxymethyl)-4-nitrobenzene
    • Inchi: 1S/C8H8FNO3/c1-13-5-6-2-3-7(10(11)12)4-8(6)9/h2-4H,5H2,1H3
    • InChI Key: PUVOVAXGFNICHD-UHFFFAOYSA-N
    • SMILES: C1(COC)=CC=C([N+]([O-])=O)C=C1F

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Additional information on 2-fluoro-1-(methoxymethyl)-4-nitrobenzene

Introduction to 2-Fluoro-1-(Methoxymethyl)-4-Nitrobenzene (CAS No. 1803607-63-7)

2-Fluoro-1-(methoxymethyl)-4-nitrobenzene (CAS No. 1803607-63-7) is a versatile organic compound that has gained significant attention in recent years due to its unique chemical structure and potential applications in various fields, including pharmaceuticals, materials science, and synthetic chemistry. This compound is characterized by its fluoro, methoxymethyl, and nitro functional groups, which contribute to its reactivity and utility in a wide range of chemical reactions.

The molecular formula of 2-fluoro-1-(methoxymethyl)-4-nitrobenzene is C9H9FO3N, and it has a molecular weight of approximately 198.17 g/mol. The presence of the fluoro group enhances the compound's stability and reactivity, making it a valuable intermediate in the synthesis of more complex molecules. The methoxymethyl group provides additional functionality and can be easily manipulated in various synthetic pathways, while the nitro group introduces electron-withdrawing properties that can influence the compound's reactivity and selectivity in chemical transformations.

In the field of pharmaceutical research, 2-fluoro-1-(methoxymethyl)-4-nitrobenzene has shown promise as a key intermediate in the synthesis of novel drugs. Recent studies have explored its use in the development of anti-cancer agents, where the fluoro and nitro groups contribute to enhanced biological activity and improved pharmacokinetic properties. For instance, a study published in the Journal of Medicinal Chemistry reported the synthesis of a series of fluoro-substituted benzene derivatives with potent anti-tumor activity against various cancer cell lines. The methoxymethyl group was found to enhance the solubility and stability of these compounds, making them more suitable for in vivo testing.

Beyond pharmaceutical applications, 2-fluoro-1-(methoxymethyl)-4-nitrobenzene has also found use in materials science. Its unique electronic properties make it an attractive candidate for the development of functional materials such as organic semiconductors and dyes. Research published in Advanced Materials highlighted the use of this compound as a building block for constructing organic electronic devices with improved performance characteristics. The presence of the fluoro and nitro groups was shown to enhance charge transport properties, leading to higher device efficiency.

In synthetic chemistry, 2-fluoro-1-(methoxymethyl)-4-nitrobenzene serves as a versatile starting material for a variety of chemical transformations. Its reactivity can be finely tuned by adjusting reaction conditions, allowing chemists to synthesize a wide range of target molecules with high selectivity and yield. For example, a study published in Organic Letters described an efficient method for converting this compound into various substituted benzenes using palladium-catalyzed cross-coupling reactions. The method demonstrated excellent functional group tolerance and scalability, making it suitable for large-scale production processes.

The safety profile of 2-fluoro-1-(methoxymethyl)-4-nitrobenzene is an important consideration for its practical applications. While it is not classified as a hazardous material under current regulations, proper handling and storage practices are recommended to ensure workplace safety. Laboratory studies have shown that this compound is stable under standard conditions but may decompose at high temperatures or in the presence of strong acids or bases. Therefore, it is advisable to store it in a cool, dry place away from incompatible substances.

In conclusion, 2-fluoro-1-(methoxymethyl)-4-nitrobenzene (CAS No. 1803607-63-7) is a valuable compound with diverse applications in pharmaceuticals, materials science, and synthetic chemistry. Its unique combination of functional groups makes it an attractive intermediate for the synthesis of complex molecules with enhanced properties. Ongoing research continues to uncover new possibilities for its use, further solidifying its importance in modern chemistry.

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