5-Hydroxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acid(CAS: 35775-49-6)

5-Hydroxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acid is a crystalline compound with a molecular weight of approximately 546.4 g/mol. It is slightly soluble in water and more soluble in organic solvents. This compound is known for its chemical stability and reactivity in various functional groups, particularly its chromone ring and sugar moiety.

5-Hydroxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acid is typically synthesized through a multi-step process involving condensation reactions, coupling of chromone and sugar moieties, and subsequent derivatization. Commonly used catalysts include boron trifluoride and sulfonic acids, yielding a high degree of selectivity and good to excellent yield.

5-Hydroxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acid is used in the pharmaceutical industry for the development of novel drugs. It is also utilized in the polymer industry for the synthesis of biodegradable polymers and in the sensor industry for developing chemical and biosensors. Additionally, it has potential applications in the semiconductor industry for certain specialized electronics.

When handling 5-Hydroxy-4-oxo-2-phenyl-4H-chromen-7-yl beta-D-glucopyranosiduronic acid, it is essential to wear appropriate 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. Spills should be cleaned up immediately using appropriate materials, and the area should be decontaminated. Always refer to the Safety Data Sheet (SDS) for detailed safety information and emergency procedures.