(S)-(2-Chloro-5-iodophenyl)(4-(tetrahydrofuran-3-yloxy)phenyl)methanone CAS:915095-87-3
The synthesis of this compound is a testament to the art of organic chemistry, requiring a series of carefully orchestrated reactions. Starting with the appropriate benzene derivative, the first step often involves the introduction of the 2-chloro-5-iodo substituent through a halogenation process. This is followed by the attachment of the tetrahydrofuran-3-yloxy group, which typically involves an etherification or substitution reaction. The final product, the (S)-(2-chloro-5-iodophenyl)(4-(tetrahydrofuran-3-yloxy)phenyl)methanone, is then isolated and purified, ready for further investigation or application. Given its intricate structure, this compound is of interest in the field of medicinal chemistry, where it may serve as a lead compound for the development of novel therapeutics. Its ability to engage in various types of chemical reactions makes it a valuable synthetic tool, potentially useful in the construction of more complex molecules. Moreover, its stereochemistry, indicated by the (S) configuration, adds another layer of complexity, as it could influence the biological activity and selectivity of the compound. In summary, the (S)-(2-chloro-5-iodophenyl)(4-(tetrahydrofuran-3-yloxy)phenyl)methanone is a remarkable organic molecule that showcases the beauty and complexity of modern organic chemistry. Its synthesis and potential applications highlight the continuous pursuit of knowledge and innovation in the field, pushing the boundaries of what is possible in organic synthesis and medicinal chemistry.
Composition | C17H14ClIO3 |
Assay | 99% |
Appearance | white powder |
CAS No. | 915095-87-3 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |