D-Arabinopyranosyl thiosemicarbazide is a chemical compound characterized by its structural features, which include a D-arabinose sugar moiety linked to a thiosemicarbazide functional group. This compound typically exhibits properties associated with both carbohydrate and thiosemicarbazide functionalities, making it of interest in various biochemical applications. It may display solubility in polar solvents due to the presence of hydroxyl groups from the sugar component, while the thiosemicarbazide part can contribute to its reactivity, particularly in coordination chemistry and biological interactions. The compound may also exhibit potential biological activities, including antimicrobial or antitumor properties, which are common in thiosemicarbazide derivatives. Its molecular structure allows for hydrogen bonding, influencing its physical properties and reactivity. As with many thiosemicarbazides, it may also participate in redox reactions, further expanding its utility in synthetic and medicinal chemistry. Overall, D-arabinopyranosyl thiosemicarbazide represents a unique intersection of carbohydrate chemistry and thiosemicarbazide reactivity.

D-ARABINOPYRANOSYL THIOSEMICARBAZIDE

154634-27-2: D-Arabinopyranosyl thiosemicarbazide is a chemical compound characterized by its structural features, which include a D-arabinose sugar moiety linked to a thiosemicarbazide functional group. This compound typically exhibits properties associated with both carbohydrate and thiosemicarbazide functionalities, making it of interest in various biochemical applications. It may display solubility in polar solvents due to the presence of hydroxyl groups from the sugar component, while the thiosemicarbazide part can contribute to its reactivity, particularly in coordination chemistry and biological interactions. The compound may also exhibit potential biological activities, including antimicrobial or antitumor properties, which are common in thiosemicarbazide derivatives. Its molecular structure allows for hydrogen bonding, influencing its physical properties and reactivity. As with many thiosemicarbazides, it may also participate in redox reactions, further expanding its utility in synthetic and medicinal chemistry. Overall, D-arabinopyranosyl thiosemicarbazide represents a unique intersection of carbohydrate chemistry and thiosemicarbazide reactivity.

CAS 154634-27-2

D-ARABINOPYRANOSYL THIOSEMICARBAZIDE

D-Arabinopyranosyl thiosemicarbazide

Ref: 7W-GC5313