3-O-(TBDPS)-6-O-(D,L-1-Ethoxyethyl)-1,2:4,5-bis-O-(1-methylethylidene)-D,L-myo-inositol

3-O-(TBDPS)-6-O-(D,L-1-Ethoxyethyl)-1,2:4,5-bis-O-(1-methylethylidene)-D,L-myo-inositol is a synthetic derivative of myo-inositol designed for use in chemical research, particularly in the fields of organic synthesis and the study of inositol chemistry. This molecule features a tert-butyldiphenylsilyl (TBDPS) protecting group at the 3-O position and an ethoxyethyl group at the 6-O position, alongside isopropylidene protections at the 1,2 and 4,5 positions. These groups enhance the molecule′s stability and reactivity, facilitating selective chemical modifications and studies on the behavior of inositols under various synthetic conditions. The use of both D and L configurations allows researchers to explore the effects of chirality on the biological activity and chemical reactivity of the compound. This compound is instrumental in advancing the understanding of polyol protection strategies, aiding in the development of more efficient synthetic routes for complex inositol-based structures. These structures are often used to study carbohydrate chemistry dynamics, mimicking natural biochemical processes in a controlled lab setting. The research applications focus on non-biological uses such as developing new materials and chemical sensors, where the unique properties of inositols can be exploited to improve functionality and performance.