The (Z)-Cycloheptadec-9-enone, also known as (Z)-18-hydroxy-9-octadecenoic acid, plays a crucial role in chemical synthesis as a key intermediate in various organic reactions. This compound serves as a versatile building block in the synthesis of complex natural products and pharmaceutical compounds. It exhibits unique reactivity due to the presence of the conjugated double bond, allowing for selective functionalization and stereocontrol in the synthesis of bioactive molecules.(Z)-Cycloheptadec-9-enone is commonly utilized in the construction of carbon-carbon bonds through cross-coupling reactions, such as the Heck reaction, Suzuki coupling, and Wittig reaction. These transformations enable the formation of new carbon-carbon bonds, facilitating the creation of intricate molecular structures with high efficiency. Additionally, this compound serves as a valuable precursor for the introduction of functional groups and stereocenters through selective chemical transformations, enabling chemists to access diverse chemical space in synthetic routes.Furthermore, (Z)-Cycloheptadec-9-enone can participate in various cyclization reactions to form cyclic compounds with intricate ring systems. The presence of the conjugated double bond imparts unique reactivity, allowing for the formation of complex ring structures with high selectivity and efficiency. This capability makes (Z)-Cycloheptadec-9-enone a valuable building block in the synthesis of natural products, pharmaceuticals, and bioactive compounds that contain cycloheptene motifs.In summary, (Z)-Cycloheptadec-9-enone serves as a versatile and highly valuable intermediate in chemical synthesis, enabling chemists to access diverse chemical space, construct complex molecular architectures, and synthesize bioactive compounds with high precision and efficiency.
sales@aaronchem.com
