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Catalog Number:
21975
CAS Number:
6974-32-9
1-O-acétyl-2,3,5-tri-o-benzoyl-β-D-ribofuranose
Purity:
≥ 98 % (HPLC)
Synonym(s):
1-Acétyl-2,3,5-tribenzoy-β-D-ribofuranose
Documents
$22.03 /5G
Taille
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Informations sur le produit

1-O-Acetyl-2,3,5-tri-o-benzoyl-b-D-ribofuranose is a versatile chemical compound widely utilized in the field of organic synthesis and carbohydrate chemistry. This compound, characterized by its unique structure, serves as an important intermediate in the synthesis of various nucleosides and nucleotides, which are essential for biochemistry and molecular biology research. Its ability to facilitate glycosylation reactions makes it particularly valuable in the development of antiviral and anticancer agents, showcasing its relevance in pharmaceutical applications.

Researchers and industry professionals appreciate the compound's stability and reactivity, which allow for efficient modifications and derivatizations. Its use in the synthesis of complex carbohydrates and glycosides opens avenues for the exploration of glycoengineering and the development of novel therapeutic agents. With its favorable properties, 1-O-Acetyl-2,3,5-tri-o-benzoyl-b-D-ribofuranose stands out as a key player in advancing research and innovation in the fields of medicinal chemistry and biotechnology.

Numéro CAS 
6974-32-9
Formule moléculaire
C 28 H 24 O 9
Poids moléculaire 
504.49
Point de fusion 
127 - 133 °C
Rotation optique 
[a] D 20 3 )
Informations générales
Numéro CAS 
6974-32-9
Formule moléculaire
C 28 H 24 O 9
Poids moléculaire 
504.49
Point de fusion 
127 - 133 °C
Rotation optique 
[a] D 20 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

1-O-Acetyl-2,3,5-tri-o-benzoyl-b-D-ribofuranose is widely utilized in research focused on:

  • Nucleoside Synthesis: This compound serves as a key intermediate in the synthesis of nucleosides, which are essential for the development of antiviral and anticancer drugs.
  • Biochemical Studies: It is used in studies involving carbohydrate chemistry, helping researchers understand sugar interactions in biological systems.
  • Drug Formulation: The compound's unique structure allows it to be incorporated into drug formulations, enhancing the stability and bioavailability of therapeutic agents.
  • Analytical Chemistry: It is employed as a standard in chromatographic techniques, aiding in the analysis of complex mixtures in pharmaceutical research.
  • Glycoconjugate Research: This chemical is instrumental in the synthesis of glycoconjugates, which play critical roles in cell signaling and immune response.

Citations