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Oct . 21, 2024 18:04 Back to list

diethyl(phenylacetyl)malonate cas 20320-59-6



Diethyl(Phenylacetyl)Malonate A Versatile Compound in Organic Synthesis


Diethyl(phenylacetyl)malonate, with the CAS number 20320-59-6, is an intriguing compound that has garnered significant attention in the field of organic chemistry. This ester is known for its unique structural features, which make it a valuable intermediate in various synthetic pathways. Understanding its properties, synthesis, and applications can provide insights into its role in organic synthesis and medicinal chemistry.


Structurally, diethyl(phenylacetyl)malonate is characterized by the presence of malonic acid and a phenylacetyl group. The compound features two ethyl ester groups flanking a malonate backbone, creating sites for nucleophilic substitution and enabling further chemical modifications. Its molecular formula is C14H16O4, indicating a relatively complex architecture conducive to diverse reactions.


One of the most significant aspects of diethyl(phenylacetyl)malonate is its utility in the synthesis of various biologically active compounds. The malonate moiety allows it to participate in classic reactions such as the Michael addition, where it can react with various nucleophiles to form new carbon-carbon bonds. This feature is critical in building complex molecules that may exhibit pharmacological activity. Furthermore, it can serve as a precursor for the synthesis of α-amino acids, which are fundamental building blocks in biochemistry and drug development.


diethyl(phenylacetyl)malonate cas 20320-59-6

diethyl(phenylacetyl)malonate cas 20320-59-6

The compound's versatility extends to its involvement in the preparation of heterocycles and other functionalized compounds. Chemists have explored its application in the development of new materials and pharmaceuticals, leveraging its reactivity to introduce various functional groups that can confer specific properties to the final products. For example, derivatization of diethyl(phenylacetyl)malonate can lead to the formation of novel compounds with enhanced therapeutic profiles.


In addition to its synthetic applications, diethyl(phenylacetyl)malonate is of interest for its potential biological activities. Research has indicated that derivatives of this compound may exhibit anti-inflammatory, analgesic, and antitumor properties. This has prompted further investigations into its mechanism of action and the potential for developing new drug candidates based on its structure.


Safety and handling of diethyl(phenylacetyl)malonate are also essential considerations. As with many chemical compounds, it is crucial to follow appropriate safety protocols in laboratory settings. This includes using personal protective equipment and working within a well-ventilated area to minimize exposure. Researchers should be aware of the compound's specific handling requirements, including its reactivity and stability under different conditions.


In conclusion, diethyl(phenylacetyl)malonate is a compound with considerable significance in the realm of organic chemistry. Its unique structure and reactivity promote its use as a versatile building block in the synthesis of a wide range of chemical entities. As ongoing research continues to unravel new methodologies and applications, diethyl(phenylacetyl)malonate is poised to remain a vital compound in the advancement of synthetic organic chemistry and drug discovery efforts. The compound exemplifies the intricate interplay between chemical structure and biological function, underscoring the importance of chemical research in addressing contemporary challenges in medicine and technology.


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