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Catalog Number:
42335
CAS Number:
108032-93-5
Phényl 2,3,4,6-tétra- O -acétyl-1-thio-α-D-mannopyranoside
Purity:
≥ 98 % (HPLC)
Documents
$374.16 /5G
Taille
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Informations sur le produit

Phenyl 2,3,4,6-tetra-O-acetyl-1-thio-a-D-mannopyranoside is a versatile glycoside that plays a significant role in various fields, particularly in organic synthesis and carbohydrate chemistry. This compound is characterized by its unique structure, which includes multiple acetyl groups that enhance its stability and reactivity. Researchers and industry professionals utilize this compound for its ability to serve as a glycosyl donor in glycosylation reactions, facilitating the synthesis of complex carbohydrates and glycoproteins. Its applications extend to the pharmaceutical industry, where it can be employed in the development of novel drug formulations and targeted delivery systems.

The compound's distinctive properties, such as its solubility and reactivity, make it an ideal candidate for use in biochemical assays and as a building block in the synthesis of bioactive molecules. Additionally, its stability under various conditions allows for a wide range of applications, from academic research to industrial processes. By incorporating Phenyl 2,3,4,6-tetra-O-acetyl-1-thio-a-D-mannopyranoside into your projects, you can leverage its unique characteristics to enhance your research outcomes and product development efforts.

Numéro CAS 
108032-93-5
Formule moléculaire
C 20 H 24 O 9 S
Poids moléculaire 
440.46
Point de fusion 
85 °C
Informations générales
Numéro CAS 
108032-93-5
Formule moléculaire
C 20 H 24 O 9 S
Poids moléculaire 
440.46
Point de fusion 
85 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Phenyl 2,3,4,6-tetra-O-acetyl-1-thio-a-D-mannopyranoside is widely utilized in research focused on:

  • Glycoscience Research: This compound serves as a valuable building block for synthesizing complex carbohydrates, aiding researchers in studying glycoproteins and glycolipids.
  • Drug Development: Its unique structure allows for the exploration of new therapeutic agents, particularly in targeting specific biological pathways, enhancing drug efficacy.
  • Bioconjugation Techniques: The compound is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutics.
  • Food Industry Applications: It can be employed in flavoring and sweetening agents, providing a natural alternative to synthetic compounds, appealing to health-conscious consumers.
  • Cosmetic Formulations: Due to its potential antioxidant properties, it is explored in cosmetic products aimed at skin health, offering benefits over traditional synthetic additives.

Citations