The chemical substance known as "α-L-Mannopyranoside, 2-propen-1-yl 6-deoxy-3-O-(phenylmethyl)-, 2-(4-methylbenzenesulfonate)" with CAS number 940274-22-6 is a glycoside derivative characterized by its mannopyranoside structure, which is a six-membered cyclic form of mannose. This compound features a propenyl group at the anomeric position, contributing to its reactivity and potential applications in organic synthesis. The presence of a phenylmethyl (benzyl) group at the 3-O position enhances its lipophilicity and may influence its biological activity. Additionally, the sulfonate group at the 2-position, specifically as a 4-methylbenzenesulfonate, provides a good leaving group, making it useful in various chemical reactions, including nucleophilic substitutions. The overall structure suggests potential applications in medicinal chemistry, particularly in the development of glycosylated compounds for therapeutic purposes. Its unique functional groups and stereochemistry may also allow for specific interactions in biological systems, warranting further investigation into its properties and potential uses.

a-L-Mannopyranoside, 2-propen-1-yl6-deoxy-3-O-(phenylmethyl)-, 2-(4-methylbenzenesulfonate)

940274-22-6: The chemical substance known as "α-L-Mannopyranoside, 2-propen-1-yl 6-deoxy-3-O-(phenylmethyl)-, 2-(4-methylbenzenesulfonate)" with CAS number 940274-22-6 is a glycoside derivative characterized by its mannopyranoside structure, which is a six-membered cyclic form of mannose. This compound features a propenyl group at the anomeric position, contributing to its reactivity and potential applications in organic synthesis. The presence of a phenylmethyl (benzyl) group at the 3-O position enhances its lipophilicity and may influence its biological activity. Additionally, the sulfonate group at the 2-position, specifically as a 4-methylbenzenesulfonate, provides a good leaving group, making it useful in various chemical reactions, including nucleophilic substitutions. The overall structure suggests potential applications in medicinal chemistry, particularly in the development of glycosylated compounds for therapeutic purposes. Its unique functional groups and stereochemistry may also allow for specific interactions in biological systems, warranting further investigation into its properties and potential uses.

Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside

<p>Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside (ABTS) is a synthetic sugar derivative that is used in the modification and synthesis of saccharides. ABTS can be modified by fluorination, glycosylation, methylation, or other modifications to produce new compounds. ABTS has a CAS number of 940274-22-6.</p>

CAS 940274-22-6

a-L-Mannopyranoside, 2-propen-1-yl6-deoxy-3-O-(phenylmethyl)-, 2-(4-methylbenzenesulfonate)

Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside

Ref: 7W-GC8580

Allyl 3-O-benzyl-2-O-p-toluenesulfonyl-a-L-rhamnopyranoside

Ref: 3D-MA07952