1H-Indol-3-yl beta-D-glucopyranosiduronic acid(CAS: 35804-66-1)

1H-Indol-3-yl beta-D-glucopyranosiduronic acid is a crystalline compound with a molecular weight of approximately 442.41 g/mol. It has low water solubility and moderate solubility in organic solvents. This compound is known for its reactivity in nucleophilic substitution reactions and its stability under acidic conditions. It is insoluble in water but soluble in most organic solvents.

1H-Indol-3-yl beta-D-glucopyranosiduronic acid is typically synthesized through a multi-step process involving the coupling of indole and glucose derivatives. Commonly, a catalytic amount of a metal catalyst such as palladium or ruthenium is used to facilitate the reaction. The selectivity and yield of the synthesis can be improved by optimizing reaction conditions such as temperature, solvent, and catalyst choice.

1H-Indol-3-yl beta-D-glucopyranosiduronic acid finds applications in the pharmaceutical industry, particularly in the development of novel drug candidates. It may also be used in the field of biotechnology for the synthesis of glycosaminoglycans and in food science as a natural sugar derivative. Its unique structure makes it suitable for use in sensor technology and as a building block in the synthesis of new materials.

When handling 1H-Indol-3-yl beta-D-glucopyranosiduronic acid, it is important to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated fume hood to minimize inhalation risk. Spills should be handled carefully using absorbent material, and the area should be thoroughly cleaned with an appropriate solvent. Always refer to the safety data sheet (SDS) for detailed handling instructions and emergency procedures.