The chemical substance known as (1R,2S,3R,4R,5R)-3,4-dihydroxy-6,8-dioxabicyclo[3.2.1]oct-2-yl 4-methylbenzenesulfonate, with the CAS number 23643-29-0, is characterized by its bicyclic structure, which includes a dioxabicyclo framework. This compound features multiple hydroxyl groups, contributing to its potential reactivity and solubility in polar solvents. The presence of a sulfonate group enhances its ionic character, making it more soluble in water and suitable for various applications, including as a reagent in organic synthesis or as a potential pharmaceutical intermediate. The stereochemistry indicated by the (1R,2S,3R,4R,5R) configuration suggests specific spatial arrangements of its substituents, which can influence its biological activity and interaction with other molecules. Overall, this compound's unique structural features and functional groups make it of interest in both synthetic chemistry and medicinal chemistry contexts.

(1R,2S,3R,4R,5R)-3,4-dihydroxy-6,8-dioxabicyclo[3.2.1]oct-2-yl 4-methylbenzenesulfonate (non-preferred name)

23643-29-0: The chemical substance known as (1R,2S,3R,4R,5R)-3,4-dihydroxy-6,8-dioxabicyclo[3.2.1]oct-2-yl 4-methylbenzenesulfonate, with the CAS number 23643-29-0, is characterized by its bicyclic structure, which includes a dioxabicyclo framework. This compound features multiple hydroxyl groups, contributing to its potential reactivity and solubility in polar solvents. The presence of a sulfonate group enhances its ionic character, making it more soluble in water and suitable for various applications, including as a reagent in organic synthesis or as a potential pharmaceutical intermediate. The stereochemistry indicated by the (1R,2S,3R,4R,5R) configuration suggests specific spatial arrangements of its substituents, which can influence its biological activity and interaction with other molecules. Overall, this compound's unique structural features and functional groups make it of interest in both synthetic chemistry and medicinal chemistry contexts.

1,6-Anhydro-4-O-p-toluenesulfonyl-β-D-glucopyranose

1,6-Anhydro-4-O-p-toluenesufonyl-b-D-glucopyranose

This modified sugar can be used in the synthesis of oligosaccharides and polysaccharides. It can also be used as a custom synthesis to introduce fluorine atoms into saccharides. This modification is useful for obtaining specific glycosylation products, such as those that are methylated or click-modified.

CAS 23643-29-0

(1R,2S,3R,4R,5R)-3,4-dihydroxy-6,8-dioxabicyclo[3.2.1]oct-2-yl 4-methylbenzenesulfonate (non-preferred name)

1,6-Anhydro-4-O-p-toluenesulfonyl-β-D-glucopyranose

Ref: IN-DA002O0Q

1,6-Anhydro-4-O-p-toluenesufonyl-b-D-glucopyranose

Ref: 7W-GC5006

1,6-Anhydro-4-O-p-toluenesufonyl-b-D-glucopyranose

Ref: 3D-MA04567