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  Ross Harder,David C. Dunand,Ian McNulty Nanoscale, 2017,9, 5686-5693
• 2. Excellent humidity sensor based on ultrathin HKUST-1 nanosheets?
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  Jacob S. Jordan,Evan R. Williams Analyst, 2021,146, 2617-2625
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• 5. Establishing new scaling relations on two-dimensional MXenes for CO2 electroreduction?
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[2-(3,5-dimethoxybenzoyl)phenyl] acetate (CAS No. 890098-98-3): A Comprehensive Overview of Its Properties and Applications

The compound [2-(3,5-dimethoxybenzoyl)phenyl] acetate (CAS No. 890098-98-3) is a chemically synthesized ester derivative that has garnered significant attention in pharmaceutical and organic chemistry research. With its unique molecular structure featuring a dimethoxybenzoyl group and an acetate moiety, this compound exhibits remarkable potential in various applications, including drug development and material science. Its systematic name, 2-(3,5-dimethoxybenzoyl)phenyl acetate, reflects its precise chemical configuration, making it a subject of interest for researchers exploring novel bioactive molecules.

In recent years, the demand for specialized organic compounds like [2-(3,5-dimethoxybenzoyl)phenyl] acetate has surged, driven by advancements in targeted drug delivery systems and green chemistry. Users frequently search for terms such as "dimethoxybenzoyl derivatives uses", "acetate esters in pharmaceuticals", and "CAS 890098-98-3 applications", highlighting the growing curiosity about its functional properties. This compound's lipophilic nature and ester linkage make it a candidate for enhancing the bioavailability of certain active ingredients, a topic widely discussed in pharmacokinetics forums.

From a synthetic perspective, [2-(3,5-dimethoxybenzoyl)phenyl] acetate is typically prepared through esterification reactions involving 3,5-dimethoxybenzoic acid and 2-hydroxyphenyl acetate. Researchers often optimize reaction conditions to achieve high yields, as noted in studies focusing on catalytic ester synthesis. The compound's melting point, solubility profile, and stability under physiological conditions are critical parameters investigated in peer-reviewed journals, addressing common queries like "how to characterize dimethoxybenzoyl compounds".

Beyond pharmaceuticals, CAS 890098-98-3 has been explored in flavor and fragrance industries due to its aromatic backbone. Its structural similarity to naturally occurring phenylpropanoids allows it to mimic certain plant-derived scents, aligning with the trend toward sustainable synthetic alternatives. Environmental considerations also play a role, with searches for "biodegradable ester compounds" rising among eco-conscious developers.

Analytical techniques such as HPLC, NMR spectroscopy, and mass spectrometry are essential for verifying the purity of [2-(3,5-dimethoxybenzoyl)phenyl] acetate. Quality control remains a priority, especially when the compound is intended for high-precision formulations. Regulatory compliance, including REACH and ICH guidelines, further underscores its safe handling protocols—a recurring theme in industry whitepapers.

Future research directions may explore structure-activity relationships (SAR) of this compound to unlock new therapeutic avenues. As computational tools like molecular docking gain traction, virtual screening of dimethoxybenzoyl-based libraries could accelerate discovery pipelines. With its multifaceted utility, [2-(3,5-dimethoxybenzoyl)phenyl] acetate exemplifies the intersection of innovation and practicality in modern chemistry.

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