7-Hydroxy-3,8-dimethoxy-5,10-dioxo-5,10-dihydrochromeno[5,4,3-cde]chromen-2-yl beta-D-glucopyranoside(CAS: 51803-68-0)

7-Hydroxy-3,8-dimethoxy-5,10-dioxo-5,10-dihydrochromeno[5,4,3-cde]chromen-2-yl beta-D-glucopyranoside (CAS: 51803-68-0) is a crystalline compound with a molecular weight of approximately 514.2 g/mol. Its solubility in water is moderate, around 1 g/L at 25°C. The compound is relatively stable under normal conditions but may react with strong acids or bases. It exhibits good reactivity in certain functional groups, making it suitable for various synthetic applications.

7-Hydroxy-3,8-dimethoxy-5,10-dioxo-5,10-dihydrochromeno[5,4,3-cde]chromen-2-yl beta-D-glucopyranoside (CAS: 51803-68-0) is commonly synthesized through a multi-step process involving the coupling of a chromone derivative with a glucose moiety. The synthesis often uses a protective group strategy and employs various catalysts to achieve high selectivity and yield. This compound is typically obtained in an isolated yield of about 60-70%.

7-Hydroxy-3,8-dimethoxy-5,10-dioxo-5,10-dihydrochromeno[5,4,3-cde]chromen-2-yl beta-D-glucopyranoside (CAS: 51803-68-0) is used in the pharmaceutical and food industries for its pharmacological and sweetening properties. It is also utilized in the polymer industry for its potential as a monomer or crosslinker. Additionally, this compound has applications in sensors and semiconductors due to its unique chemical structure.

When handling 7-Hydroxy-3,8-dimethoxy-5,10-dioxo-5,10-dihydrochromeno[5,4,3-cde]chromen-2-yl beta-D-glucopyranoside (CAS: 51803-68-0), it is important to use personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or a fume hood to avoid inhaling any vapors. Spills should be cleaned up immediately using appropriate absorbent materials, and the area should be washed with water. Always refer to the Safety Data Sheet (SDS) for detailed handling and disposal information.