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4-Iodo-1-chloro-2-(4-ethoxybenzyl)benzene CAS:1103738-29-9

Synthesized through specialized organic methods, 4-iodo-1-chloro-2-(4-ethoxybenzyl)benzene features a complex structure crucial for its various applications. The presence of iodo, chloro, and 4-ethoxybenzyl substituents on the benzene ring influences its chemical reactivity, solubility, and interactions in biological systems. These structural characteristics are fundamental for understanding its pharmacological profile and potential therapeutic uses.


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Application and Effect:

This compound holds promise in pharmaceutical research owing to its structural composition. Benzene derivatives have been explored for their diverse pharmacological activities, including antimicrobial, anti-inflammatory, and anticancer properties. The specific combination of iodo, chloro, and 4-ethoxybenzyl groups may enhance its biological activity and affect its mode of action, making it a candidate for future drug development. Biological Activity and Mechanisms Studies suggest that benzene derivatives interact with biological targets due to their structural similarity to endogenous compounds or specific receptors. The iodo and chloro substitutions, along with the 4-ethoxybenzyl group, potentially modulate its binding affinity and metabolic pathways, influencing its effectiveness and safety profile. Understanding these mechanisms is critical for optimizing therapeutic outcomes. Synthetic Routes and Development The synthesis of 4-iodo-1-chloro-2-(4-ethoxybenzyl)benzene involves intricate organic processes starting from commercially available starting materials. Refining synthetic routes is essential to achieving high purity and yields, crucial for industrial-scale production and pharmaceutical applications. Moreover, optimizing synthesis pathways enhances cost-effectiveness and sustainability, key considerations in drug discovery and development. Current Research and Future Directions Current research efforts focus on exploring the compound's comprehensive biological activities, including its potential as an antimicrobial agent or its efficacy in combating inflammatory conditions. Future studies may investigate structural modifications to improve its pharmacokinetic profile or enhance specificity towards particular disease targets. Furthermore, ongoing research aims to validate its safety and efficacy through rigorous preclinical and clinical evaluations. Conclusion In conclusion, 4-iodo-1-chloro-2-(4-ethoxybenzyl)benzene represents a notable compound in organic chemistry and pharmaceutical research due to its distinctive chemical structure and potential therapeutic applications. Its incorporation of iodo, chloro, and 4-ethoxybenzyl groups into a benzene framework underscores its pharmacological promise and versatility. Advancing our understanding of its chemical behavior, biological interactions, and synthetic pathways is crucial for harnessing its full therapeutic potential and advancing its applications in medicine and related fields.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C15H14ClIO
Assay 99%
Appearance white powder
CAS No.  1103738-29-9
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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