(S)-2,3-Dihydro-1H-inden-1-ol CAS:25501-32-0

(S)-2,3-Dihydro-1H-inden-1-ol has several important applications in organic synthesis and pharmaceutical research. Here are some common uses of this compound: Medicinal Chemistry: The compound serves as a valuable building block for the synthesis of biologically active molecules. It can be utilized in the development of potential drugs targeting various therapeutic areas such as cardiovascular diseases, neurological disorders, or inflammation. Chiral Building Block: (S)-2,3-Dihydro-1H-inden-1-ol's chirality makes it an important chiral building block. It can be used to introduce chirality into a molecule, enabling the synthesis of enantiopure compounds with specific biological activities. Cycloaddition Reactions: The conjugated system of (S)-2,3-Dihydro-1H-inden-1-ol allows for cycloaddition reactions, such as Diels-Alder or [4+2] cycloadditions. These reactions enable the formation of complex ring systems, which are important in the synthesis of natural products and pharmaceutical compounds. Asymmetric Synthesis: The chiral nature of (S)-2,3-Dihydro-1H-inden-1-ol makes it useful for asymmetric synthesis. It can serve as a chiral auxiliary or ligand in asymmetric transformations, allowing for the selective formation of one enantiomer over the other. Flavor and Fragrance Industry: (S)-2,3-Dihydro-1H-inden-1-ol finds utility in the flavor and fragrance industry. Its unique structure imparts specific aromas or flavors, and it can be used as a starting material for the synthesis of fragrance compounds. Natural Product Synthesis: The indenol scaffold present in (S)-2,3-Dihydro-1H-inden-1-ol is found in various natural products with biological activity. It can be used as a starting point to synthesize or modify natural product analogs for further study. Pharmacological Studies: (S)-2,3-Dihydro-1H-inden-1-ol can be used in pharmacological studies to investigate its biological activity or evaluate its potential as a lead compound. It can be screened against various targets to assess its effects and mechanisms of action. In summary, (S)-2,3-Dihydro-1H-inden-1-ol is a versatile compound with various applications in organic synthesis and pharmaceutical research. It plays a critical role in medicinal chemistry, chiral building blocks, cycloaddition reactions, asymmetric synthesis, the flavor and fragrance industry, natural product synthesis, and pharmacological studies. The compound's high purity, stability, and ability to introduce chirality make it valuable in the development of biologically active compounds and the exploration of synthetic methodologies.