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4-fluoro-2-Methoxy-5-nitroaniline CAS:1421372-66-8

4-Fluoro-2-methoxy-5-nitroaniline is a chemical compound known for its aromatic structure comprising a nitro group, a fluoro substituent, and a methoxy group attached to an aniline ring. This configuration gives it distinctive chemical properties suitable for various applications in organic synthesis and pharmaceutical research. Synthesized through established organic chemistry methods, this compound serves as a fundamental building block for creating specialized materials and pharmaceutical intermediates, leveraging its unique structural features.


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Application and Effect:

The molecular structure of 4-fluoro-2-methoxy-5-nitroaniline integrates an aniline backbone with specific substitutions—a fluoro group at position 4, a methoxy group at position 2, and a nitro group at position 5. This arrangement influences its chemical behavior, such as acidity, reactivity in aromatic substitution reactions, and interactions in biological systems. These properties are crucial in designing molecules for targeted applications in drug discovery and material science. Synthesis Methods and Applications Synthesis of 4-fluoro-2-methoxy-5-nitroaniline typically involves sequential functionalization of aniline derivatives under controlled conditions. Key steps include diazotization, nitration, and selective substitution reactions to introduce the fluoro and methoxy groups. The synthesis pathway underscores its utility as a versatile intermediate in organic chemistry, enabling further derivatization for specific industrial and pharmaceutical applications. Pharmacological and Material Science Relevance In pharmaceutical research, this compound serves as a valuable intermediate for developing potential drug candidates, particularly in designing molecules with enhanced biological activities or specific receptor interactions. Its substituted aromatic ring can influence pharmacokinetic properties and therapeutic efficacy, making it a promising candidate in medicinal chemistry. Additionally, in material science, its unique substitution pattern lends itself to applications in dyes, pigments, and advanced materials requiring tailored chemical properties. Environmental and Technological Applications Beyond pharmaceuticals and materials science, 4-fluoro-2-methoxy-5-nitroaniline holds promise in environmental applications, such as the development of sensors or catalysts for detecting and remedying pollutants. Its structural versatility allows modifications aimed at improving efficiency and selectivity in various chemical processes, contributing to environmental sustainability and technological innovation. Conclusion 4-Fluoro-2-methoxy-5-nitroaniline stands out as a versatile compound with significant applications in organic synthesis, pharmaceutical research, and material science. Its unique molecular structure, coupled with precise synthesis methodologies, underscores its importance as a foundational component for developing novel pharmaceuticals, functional materials, and environmental solutions. Continued research efforts are likely to focus on optimizing synthesis routes, exploring new applications, and uncovering additional benefits across scientific and industrial domains.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C7H7FN2O3
Assay 99%
Appearance white powder
CAS No.  1421372-66-8
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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