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4-Fluoro-3-nitrotoluene CAS:446-11-7

4-Fluoro-3-nitrotoluene is an aromatic compound with the molecular formula C7H6ClN2O2. It consists of a toluene backbone substituted with a nitro group (–NO2) at the 3-position and a fluorine atom (–F) at the 4-position. This compound is notable for its unique electronic properties, resulting from the combination of the electron-withdrawing nitro group and the electronegative fluorine atom. Due to these attributes, 4-fluoro-3-nitrotoluene serves as an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds.


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Application and Effect:

4-Fluoro-3-nitrotoluene is an aromatic compound with the molecular formula C7H6ClN2O2. It consist4-Fluoro-3-nitrotoluene is an aromatic nitro compound that has gained attention in various fields, including organic synthesis, materials science, and medicinal chemistry. The compound features a methyl group attached to a benzene ring, which enhances its reactivity and facilitates its use as a precursor in multiple chemical transformations. One of the primary applications of 4-fluoro-3-nitrotoluene lies in its role as an intermediate in pharmaceutical synthesis. The presence of both the nitro and fluoro groups makes this compound particularly valuable for developing biologically active molecules. Nitrogen-containing heterocycles derived from 4-fluoro-3-nitrotoluene have been shown to exhibit promising pharmacological activities, such as anti-inflammatory and antimicrobial effects. By strategically modifying the compound’s structure, researchers can create a diverse array of derivatives tailored for specific therapeutic targets. In addition to its pharmaceutical applications, 4-fluoro-3-nitrotoluene is also significant in the agrochemical industry. Its synthetic versatility enables the formation of herbicides and pesticides that are effective against a wide range of agricultural pests. The incorporation of the nitro group significantly enhances the biological activity of the resulting compounds, making them suitable for crop protection. The compound's unique combination of functional groups also opens avenues for its incorporation into advanced materials. For instance, incorporating 4-fluoro-3-nitrotoluene into polymers can enhance their thermal stability, mechanical strength, and resistance to chemicals. This adaptability makes it a candidate for specialized coatings and adhesives used in industries requiring durable and resilient materials. Synthetically, 4-fluoro-3-nitrotoluene can be obtained through various methods, including electrophilic aromatic substitution reactions, where the introduction of the nitro and fluoro groups can be carefully controlled. The accessibility of this compound is crucial for both research and industrial applications, as it allows chemists to explore further modifications and potential uses. Moreover, ongoing research focuses on optimizing the synthesis of 4-fluoro-3-nitrotoluene using greener methodologies to reduce environmental impact and improve sustainability in chemical production. These approaches aim to minimize hazardous reagents and solvents, aligning with contemporary trends toward eco-friendly practices in the chemical industry. In conclusion, 4-fluoro-3-nitrotoluene is a versatile compound with broad applications across pharmaceuticals, agrochemicals, and materials science. Its unique structural features facilitate various chemical transformations, enabling the production of a wide range of valuable derivatives. As research progresses, the significance of 4-fluoro-3-nitrotoluene is expected to grow, contributing to advancements in drug discovery, agricultural innovation, and the development of high-performance materials.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C7H6FNO2
Assay 99%
Appearance white powder
CAS No.  446-11-7
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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