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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzamides
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzoic acids and derivatives Benzamides

Comprehensive Overview of 4-Ethoxybenzamide (CAS No. 55836-71-0): Properties, Applications, and Industry Insights

4-Ethoxybenzamide (CAS No. 55836-71-0), a specialized organic compound, has garnered significant attention in pharmaceutical and chemical research due to its unique structural properties and versatile applications. This benzamide derivative is characterized by an ethoxy group (-OCH₂CH₃) attached to the benzene ring, which enhances its solubility and reactivity. Researchers and manufacturers frequently search for "4-Ethoxybenzamide synthesis," "CAS 55836-71-0 uses," and "benzamide derivatives in medicine," reflecting its relevance in modern science.

The compound’s molecular formula, C₉H₁₁NO₂, and a molar mass of 165.19 g/mol, make it a candidate for intermediate synthesis in drug development. Its crystalline form and stability under standard conditions are often highlighted in queries like "4-Ethoxybenzamide physical properties" and "safe handling of CAS 55836-71-0." Notably, its low toxicity profile aligns with the growing demand for eco-friendly chemical alternatives, a trending topic in green chemistry forums.

In pharmaceuticals, 4-Ethoxybenzamide serves as a precursor for analgesics and anti-inflammatory agents. Recent studies explore its potential in "neuropathic pain management" and "non-opioid pain relief," addressing current concerns about opioid dependency. The compound’s mechanism of action, often compared to salicylamide derivatives, is a hot topic in medicinal chemistry discussions. Additionally, its role in "cosmetic stabilizers" and "UV-filter enhancers" has gained traction in cosmetic science, linking to the booming clean beauty movement.

From an industrial perspective, CAS 55836-71-0 is utilized in polymer stabilization and agrochemical formulations. Searches for "4-Ethoxybenzamide in crop protection" and "polymer additive compatibility" underscore its cross-sector utility. Analytical methods like HPLC and GC-MS are frequently employed for purity assessment, as noted in queries such as "analytical testing of benzamide compounds." Regulatory compliance, including REACH and FDA guidelines, is another critical area, with professionals seeking "4-Ethoxybenzamide safety data sheets."

Emerging trends highlight 4-Ethoxybenzamide’s potential in personalized medicine and biodegradable materials, aligning with the global push for sustainability. Researchers are investigating its enantioselective synthesis, responding to queries like "chiral separation of 4-Ethoxybenzamide." The compound’s compatibility with continuous flow chemistry—a technique gaining popularity for scalable production—further enhances its industrial appeal.

In summary, 4-Ethoxybenzamide (CAS No. 55836-71-0) bridges multiple scientific disciplines, from drug discovery to material science. Its adaptability to green chemistry principles and alignment with healthcare innovation positions it as a compound of enduring interest. As industries pivot toward sustainable solutions, the demand for detailed resources on "4-Ethoxybenzamide applications" and "CAS 55836-71-0 suppliers" is expected to rise, making this overview a timely reference for professionals and academics alike.

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