N-(2-Chloro-4-fluoro-6-methylphenyl)acetamide CAS:1710696-26-6
N-(2-Chloro-4-fluoro-6-methylphenyl)acetamide finds extensive application in organic synthesis, particularly in the preparation of biologically active compounds and pharmaceutical intermediates. Its chloro- and fluoro-substituted phenyl ring, along with the acetamide functional group, imparts specific properties to the molecules synthesized from it, influencing their biological activity and pharmacokinetic profiles. In medicinal chemistry, this compound serves as a crucial building block for the synthesis of potential drug candidates targeting various diseases and conditions. Researchers utilize its unique structure to design molecules with desired pharmacological properties, such as enhanced potency, selectivity, or metabolic stability. Moreover, N-(2-Chloro-4-fluoro-6-methylphenyl)acetamide is employed in academic and industrial laboratories for exploring new synthetic routes and methodologies. Its versatile nature allows chemists to access diverse chemical space, facilitating the discovery and optimization of novel compounds with therapeutic potential. Additionally, this compound may be utilized in agrochemical research for the development of pesticides or herbicides. By incorporating N-(2-Chloro-4-fluoro-6-methylphenyl)acetamide into molecular structures, scientists aim to design agricultural chemicals with improved efficacy and environmental safety profiles. Overall, N-(2-Chloro-4-fluoro-6-methylphenyl)acetamide plays a significant role in organic synthesis and drug discovery efforts, contributing to advancements in both medicinal and agricultural sciences. Its distinctive molecular properties make it a valuable resource for researchers seeking to develop innovative solutions for various societal challenges.
Composition | C9H9ClFNO |
Assay | 99% |
Appearance | white powder |
CAS No. | 1710696-26-6 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |