Ethyl 2-(3-chlorobenzoyl)butanoate

Ethyl 2-(3-chlorobenzoyl)butanoate, with the CAS number 1282994-87-9, is a highly versatile and pure chemical compound that holds immense potential for researchers and scientists across various fields. This Halogenated Compound, featuring a chlorine substituent on the benzoyl moiety, offers a unique set of properties that make it a valuable asset in pharmaceutical, agrochemical, and material science applications.

At the heart of this compound lies a carefully crafted molecular structure, with a chemical formula of C13H15ClO3 and a molecular weight of 254.71 g/mol. The presence of the chloro group, along with the ester functionality, endows Ethyl 2-(3-chlorobenzoyl)butanoate with a distinct reactivity profile, allowing it to serve as a versatile building block in a wide range of chemical transformations and synthetic endeavors.

The high purity of this compound, with a minimum of 95% as per the provided specifications, ensures reliable and consistent results in research and development projects. Its MDL number, MFCD16502403, provides a unique identifier for researchers seeking detailed information about this chemical entity.

Pharmaceutical Research

In the realm of pharmaceutical research, Ethyl 2-(3-chlorobenzoyl)butanoate finds its niche as a valuable intermediate in the synthesis of novel drug candidates. Its distinct structural features and reactivity patterns allow chemists to incorporate it into the design and development of innovative therapeutics, targeting a diverse array of health conditions. The chloro-substituted benzoyl moiety, combined with the ester functionality, offers opportunities for further functionalization and optimization, ultimately leading to the creation of more effective and selective pharmaceutical compounds.

Agrochemical Applications

The agricultural industry also benefits from the unique properties of Ethyl 2-(3-chlorobenzoyl)butanoate. This compound serves as a building block in the synthesis of advanced crop protection agents, such as pesticides and herbicides. The chloro substituent, along with the ester group, can contribute to the development of more potent and selective agrochemicals, helping to safeguard crops, improve yields, and minimize environmental impact.

Material Science Innovations

Beyond the pharmaceutical and agrochemical realms, Ethyl 2-(3-chlorobenzoyl)butanoate also finds applications in the field of material science. Researchers in this domain utilize the unique properties of this compound to engineer novel materials with enhanced performance characteristics. The chloro-substituted benzoyl moiety and the ester functionality can be leveraged to create polymers, coatings, or other advanced materials with improved thermal stability, mechanical strength, or optical properties, opening up new possibilities in various industries.

Handling and Storage

To ensure the long-term stability and purity of Ethyl 2-(3-chlorobenzoyl)butanoate, it is recommended to store the compound in a cool, dry, and well-ventilated environment. Proper handling procedures, including the use of personal protective equipment, should be followed to minimize any potential risks associated with the compound's handling. For more detailed information on safety guidelines and storage conditions, please consult the technical inquiry form on the product page.

Unlock the Potential

Ethyl 2-(3-chlorobenzoyl)butanoate, with its exceptional purity and versatile chemical properties, presents a wealth of opportunities for researchers and scientists across various disciplines. Whether you are exploring new pharmaceutical avenues, developing innovative agrochemicals, or engineering advanced materials, this compound can be a valuable asset in your endeavors. Unlock the potential of Ethyl 2-(3-chlorobenzoyl)butanoate and embark on a journey of discovery, pushing the boundaries of scientific innovation.