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Catalog Number:
21975
CAS Number:
6974-32-9
1-O-Acetil-2,3,5-tri-o-benzoil-β-D-ribofuranosa
Purity:
≥ 98 % (HPLC)
Synonym(s):
1-Acetil-2,3,5-tribenzoil-β-D-ribofuranosa
Documents
$22.03 /5G
Tamaño
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Información del producto

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.

Número CAS
6974-32-9
Fórmula molecular
C28H24O9
Peso molecular
504.49
Número MDL
MFCD00005357
Punto de fusión
127 - 133 °C
Rotación óptica
[a] D20 3 )
Condiciones
Tienda en RT
Información general
Número CAS
6974-32-9
Fórmula molecular
C28H24O9
Peso molecular
504.49
Número MDL
MFCD00005357
Punto de fusión
127 - 133 °C
Rotación óptica
[a] D20 3 )
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

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.

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