2-Hydroxy-4-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl beta-D-glucopyranoside(CAS: 20229-56-5)

2-Hydroxy-4-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl beta-D-glucopyranoside is a crystalline compound with a molecular weight of approximately 534.45 g/mol. It has a moderate solubility in water and is practically insoluble in organic solvents. The compound is highly reactive towards hydrolysis and exhibits good stability under acidic conditions. It can form hydrogen bonds due to its hydroxyl groups, contributing to its crystalline nature.

2-Hydroxy-4-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl beta-D-glucopyranoside is typically synthesized through a multi-step process involving glucopyranosylation and chromone formation. Commonly, the synthesis involves the use of acetyl glucosamine and 2-acetyl-3,5,7-trihydroxy-4-oxo-4H-chromen-2-one as starting materials. The reaction is catalyzed by an enzyme or a chemical catalyst, achieving high selectivity and yield under mild conditions.

2-Hydroxy-4-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl beta-D-glucopyranoside is utilized in the pharmaceutical and biomedical industries for its potential as a bioactive compound. It can be applied in the development of new drugs and as a research tool in biological assays. Additionally, it may find applications in the food industry as a natural colorant or antioxidant, though its specific uses are limited due to its complexity.

When handling 2-Hydroxy-4-(3,5,7-trihydroxy-4-oxo-4H-chromen-2-yl)phenyl beta-D-glucopyranoside, it is essential to use Personal Protective Equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a fume hood to minimize inhalation exposure. Spills should be cleaned up carefully, and the material should be disposed of according to local regulations. It is advisable to refer to the Safety Data Sheet (SDS) for specific handling instructions and emergency procedures.