CAS 63064-49-3

Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside

Description:

Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside, with CAS number 63064-49-3, is a glycoside derivative characterized by its complex structure, which includes an allyl group, an acetylamino moiety, and a glucopyranoside backbone. This compound features a phenylmethylene group that contributes to its aromatic characteristics, enhancing its potential for various chemical interactions. The presence of the acetylamino group suggests that it may exhibit biological activity, possibly influencing its solubility and reactivity. The glucopyranoside structure indicates that it is a sugar derivative, which may play a role in its interaction with biological systems, such as enzymes or receptors. The compound is likely to be soluble in organic solvents, and its stability can be influenced by factors such as pH and temperature. Overall, this substance may have applications in medicinal chemistry, particularly in the development of glycosylated compounds with potential therapeutic properties.

Formula: C₁₈H₂₃NO₆

Synonyms:

• Allyl-2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside
• 2-Propenyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside
• Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-a-D-glucopyranoside
• α-D-Glucopyranoside, 2-propen-1-yl 2-(acetylaMino)-2-deoxy-4,6-O-(phenylMethylene)-
• 2-Propenyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-a-D-glucopyranoside
• Allyl 2-acetamido-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside
• Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside

Allyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside

CAS: 63064-49-3

Allyl 2-(acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside is a biochemical reagent used in glycobiology research. Glycobiology focuses on studying the structure, synthesis, biology, and evolution of carbohydrates. It encompasses carbohydrate chemistry, the enzymology of glycan formation and degradation, protein-glycan recognition, and the roles of glycans in biological systems, and it is closely linked to fundamental research, biomedicine, and biotechnology.

Formula: C₁₈H₂₃NO₆

Color and Shape: Solid

Molecular weight: 349.38

Ref: TM-TSW-00633

Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside

CAS: 63064-49-3

Molecular weight: 349.38

Ref: 7W-GC3034

Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-Alpha-D-glucopyranoside

Controlled Product

CAS: 63064-49-3

Applications Allyl 2-(Acetylamino)-2-deoxy-4,6-O-(phenylmethylene)-α-D-glucopyranoside (cas# 63064-49-3) is a compound useful in organic synthesis.

Formula: C₁₈H₂₃NO₆

Color and Shape: Neat

Molecular weight: 349.38

Ref: TR-A549200

Allyl 2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside

CAS: 63064-49-3

Allyl 2-acetamido-4,6,-O-benzylidene-2-deoxy-a-D-glucopyranoside is a sugar that is used as a custom synthesis or modification. It is also called allyl 2-(1,3-dioxo-1,3,4,-thiadiazolidinium)acetamido 4,6,-O-(benzylidene)-2 deoxy erythro -a D glucopyranoside. Allyl 2 acetamido 4,6,-O -benzylidene -2 deoxy erythro -a D glucopyranoside is used in the glycosylation of proteins and oligosaccharides and in the synthesis of saccharides. This compound has been shown to be useful in identifying glycosaminoglycan chains in complex carbohydrates.

Formula: C₁₈H₂₃NO₆

Purity: Min. 95%

Molecular weight: 349.39 g/mol

Ref: 3D-MA09591