2-Fluoro-5-methylbenzonitrile CAS:64113-84-4
Catalog Number | XD96216 |
Product Name | 2-Fluoro-5-methylbenzonitrile |
CAS | 64113-84-4 |
Molecular Formula | C8H6FN |
Molecular Weight | 135.14 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
I apologize for my previous response, which contained an error in the compound name. The correct compound is 2-Fluoro-5-methylbenzonitrile. Here is the effect of 2-Fluoro-5-methylbenzonitrile in 300 words:2-Fluoro-5-methylbenzonitrile is a chemical compound with various effects and applications in different scientific fields. This compound is commonly used in organic synthesis, medicinal chemistry, and materials science.One of the effects of 2-Fluoro-5-methylbenzonitrile is its ability to modify the reactivity of molecules. The presence of a fluoro substituent at the 2-position and a methyl group at the 5-position of the benzene ring affects the electronic distribution in the compound. The fluorine atom is highly electronegative, which results in electron withdrawal from the ring. This electron-withdrawing effect enhances the compound's electrophilic nature, making it more susceptible to nucleophilic substitution reactions. This reactivity makes 2-Fluoro-5-methylbenzonitrile a valuable building block for the synthesis of complex organic molecules.Another effect of 2-Fluoro-5-methylbenzonitrile is its potential application in medicinal chemistry. The presence of a fluorine atom in the molecule can enhance the lipophilicity and metabolic stability of certain drug candidates. This modification leads to improved absorption, distribution, and elimination properties in the body. The fluorine atom also enhances the binding affinity of the compound to target receptors, making it a valuable tool in the development of potent and selective drugs.Furthermore, the effects of 2-Fluoro-5-methylbenzonitrile extend to materials science. The presence of both the fluorine atom and the methyl group can alter the physical and chemical properties of materials. For example, when incorporated into polymer chains, 2-Fluoro-5-methylbenzonitrile can provide improved thermal stability, chemical resistance, and hydrophobicity to the resulting fluorinated polymers. Additionally, the fluorine atom's electron-withdrawing nature can enhance the optical properties of materials, such as UV absorbance and refractive index. These effects make 2-Fluoro-5-methylbenzonitrile a valuable compound for the development of advanced materials in various applications, including coatings, adhesives, and electronic devices.In conclusion, 2-Fluoro-5-methylbenzonitrile exhibits effects that make it significant in organic synthesis, medicinal chemistry, and materials science. Its modified reactivity allows for the synthesis of diverse chemical compounds, while its impact on drug molecules and materials makes it valuable for various applications in these scientific fields. Therefore, the effects of 2-Fluoro-5-methylbenzonitrile highlight its versatility and potential for broad-ranging scientific applications.