The chemical substance with the name "[(3S,4R,5S,6R)-5-acetamido-3,4-diacetoxy-6-allyloxy-tetrahydropyran-2-yl]methyl acetate" and CAS number 28738-44-5 is a complex organic compound characterized by its tetrahydropyran ring structure, which is a six-membered cyclic ether. This compound features multiple functional groups, including acetamido, diacetoxy, and allyloxy moieties, contributing to its reactivity and potential applications in organic synthesis or medicinal chemistry. The stereochemistry indicated by the (3S,4R,5S,6R) configuration suggests specific spatial arrangements of atoms, which can significantly influence the compound's biological activity and interaction with other molecules. The presence of acetoxy groups may enhance its solubility and reactivity, while the allyloxy group can provide sites for further chemical modifications. Overall, this compound's unique structural features make it of interest for research in various fields, including pharmaceuticals and materials science, where its properties can be exploited for specific applications.

[(3S,4R,5S,6R)-5-acetamido-3,4-diacetoxy-6-allyloxy-tetrahydropyran-2-yl]methyl acetate

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Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a synthetic glycoside that can be used as a building block for the synthesis of oligosaccharides and polysaccharides. It has been shown to have high purity and custom synthesis. This molecule is fluorinated at the 3 position and glycosylated at the 4 position. Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D--glucopyranoside is also methylated at the 6 position.

CAS 28738-44-5: [(3S,4R,5S,6R)-5-acetamido-3,4-diacetoxy-6-allyloxy-tetrahydropyran-2-yl]methyl acetate

Allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside

Ref: 3D-MA08997

β-D-Glucopyranoside, 2-propen-1-yl 2-(acetylamino)-2-deoxy-, 3,4,6-triacetate

Ref: IN-DA002WB9

Allyl 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside

Ref: 7W-GC3660