4-Aminophenyl 1-thio-β-D-cellobioside is a chemical compound characterized by its structure, which includes an aminophenyl group linked to a cellobioside moiety via a thioether bond. This compound is typically used in biochemical research, particularly in studies involving glycosylation and carbohydrate chemistry. The presence of the amino group suggests potential reactivity, allowing for further derivatization or conjugation in synthetic applications. The thioether linkage imparts unique properties, such as increased stability compared to other glycosidic bonds, and may influence the compound's solubility and interaction with biological systems. As a cellobioside derivative, it may exhibit specific biological activities, potentially serving as a substrate for glycosidases or as a probe in enzyme studies. Its CAS number, 68636-51-1, allows for precise identification in chemical databases and literature. Overall, this compound represents a valuable tool in the exploration of carbohydrate-related processes and the development of glycomimetics.

4-AMINOPHENYL 1-THIO-§-D-CELLOBIOSIDE

68636-51-1: 4-Aminophenyl 1-thio-β-D-cellobioside is a chemical compound characterized by its structure, which includes an aminophenyl group linked to a cellobioside moiety via a thioether bond. This compound is typically used in biochemical research, particularly in studies involving glycosylation and carbohydrate chemistry. The presence of the amino group suggests potential reactivity, allowing for further derivatization or conjugation in synthetic applications. The thioether linkage imparts unique properties, such as increased stability compared to other glycosidic bonds, and may influence the compound's solubility and interaction with biological systems. As a cellobioside derivative, it may exhibit specific biological activities, potentially serving as a substrate for glycosidases or as a probe in enzyme studies. Its CAS number, 68636-51-1, allows for precise identification in chemical databases and literature. Overall, this compound represents a valuable tool in the exploration of carbohydrate-related processes and the development of glycomimetics.

Stability Store Under Argon Applications Shown to be a functional affinity ligand for the separation of exo-(cellobiohydrolasees) and endo-(endoglucanases) acting cellulases. References Piyachomkwan, K., et al.: Carbohydrate Research, 303, 255 (1997)

CAS 68636-51-1

4-AMINOPHENYL 1-THIO-§-D-CELLOBIOSIDE

4-Aminophenyl 1-Thio-b-D-cellobioside

Ref: TR-A626960