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Diethyl ethylphenylmalonate CAS: 76-67-5

Short Description:

Catalog Number: XD93739
Cas: 76-67-5
Molecular Formula: C15H20O4
Molecular Weight: 264.32
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Product Tags

Catalog Number XD93739
Product Name Diethyl ethylphenylmalonate
CAS 76-67-5
Molecular Formula C15H20O4
Molecular Weight 264.32
Storage Details Ambient

 

Product Specification

Appearance White powder
Assay 99% min

 

Diethyl ethylphenylmalonate, also known as malonic ester, is a versatile compound widely utilized in organic synthesis. It consists of an ester group and two ethyl groups attached to a malonic acid derivative, with a phenyl group further substituted on the alpha-carbon. This unique structural arrangement enables a multitude of applications in various chemical reactions.One primary use of diethyl ethylphenylmalonate is as a precursor for the synthesis of carboxylic acids. Through a process called malonic ester synthesis, diethyl ethylphenylmalonate can undergo nucleophilic substitution reactions, where one or both of the ester groups are replaced with other functional groups. The resulting intermediates can then be hydrolyzed to yield carboxylic acids with specific modifications or structural features. This synthetic approach is particularly valuable in the pharmaceutical industry for the creation of drug molecules and intermediates with tailored properties and functionalities.Diethyl ethylphenylmalonate also serves as a useful building block for the synthesis of various heterocyclic compounds. The malonic ester moiety can participate in condensation reactions to form cyclic structures, such as pyrazoles, pyrimidines, or pyridines. These heterocyclic compounds are essential in the development of pharmaceuticals, agrochemicals, and materials chemistry. The presence of the phenyl group in diethyl ethylphenylmalonate adds additional aromatic character and diversity to the resulting heterocycles, contributing to their unique properties.Furthermore, diethyl ethylphenylmalonate plays a crucial role as a Michael acceptor in organic reactions. The alpha-carbon adjacent to the phenyl group is electrophilic, making it prone to nucleophilic attack by various reagents. This reactivity allows diethyl ethylphenylmalonate to participate in Michael addition reactions, where it forms covalent bonds with nucleophiles such as amines or thiols. These reactions are widely exploited in the synthesis of pharmaceuticals, natural product derivatives, and advanced chemical building blocks.In summary, diethyl ethylphenylmalonate is a versatile compound used in organic synthesis for its ability to undergo various chemical transformations. Its applications range from the synthesis of carboxylic acids to the formation of heterocyclic compounds, as well as participation in Michael addition reactions. With its ester group, phenyl group, and malonic acid derivative, diethyl ethylphenylmalonate offers chemists a valuable tool for building diverse molecules and functionalizing complex structures in multiple fields, including pharmaceuticals, agrochemicals, and materials chemistry.


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    Diethyl ethylphenylmalonate CAS: 76-67-5