1,5-Anhydro-2-deoxy-4-O-beta-D-glucopyranosyl-D-arabino-hex-1-enitol, with CAS number 490-51-7, is a carbohydrate derivative characterized by its unique structural features. This compound is a sugar alcohol that contains an anhydro sugar moiety, which contributes to its stability and solubility in water. It features a glucopyranosyl group linked to an arabino-hex-1-enitol structure, indicating the presence of both pyranose and furanose forms in its molecular architecture. The compound exhibits properties typical of sugars, such as sweetness and the ability to participate in various biochemical reactions, including glycosylation. Its anhydro form suggests a potential for reduced reactivity compared to its hydrated counterparts. Additionally, it may play a role in biological systems, possibly influencing metabolic pathways or serving as a precursor for other biochemical compounds. The presence of hydroxyl groups in its structure allows for hydrogen bonding, which can affect its solubility and interaction with other molecules. Overall, this compound is of interest in both biochemical research and potential applications in pharmaceuticals or food science.

1,5-anhydro-2-deoxy-4-O-beta-D-glucopyranosyl-D-arabino-hex-1-enitol

490-51-7: 1,5-Anhydro-2-deoxy-4-O-beta-D-glucopyranosyl-D-arabino-hex-1-enitol, with CAS number 490-51-7, is a carbohydrate derivative characterized by its unique structural features. This compound is a sugar alcohol that contains an anhydro sugar moiety, which contributes to its stability and solubility in water. It features a glucopyranosyl group linked to an arabino-hex-1-enitol structure, indicating the presence of both pyranose and furanose forms in its molecular architecture. The compound exhibits properties typical of sugars, such as sweetness and the ability to participate in various biochemical reactions, including glycosylation. Its anhydro form suggests a potential for reduced reactivity compared to its hydrated counterparts. Additionally, it may play a role in biological systems, possibly influencing metabolic pathways or serving as a precursor for other biochemical compounds. The presence of hydroxyl groups in its structure allows for hydrogen bonding, which can affect its solubility and interaction with other molecules. Overall, this compound is of interest in both biochemical research and potential applications in pharmaceuticals or food science.

CAS 490-51-7

1,5-anhydro-2-deoxy-4-O-beta-D-glucopyranosyl-D-arabino-hex-1-enitol

Cellobial

Ref: IN-DA003P8X

D-Cellobial

Ref: 3D-OC14037