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Catalog Number:
29110
CAS Number:
4594-52-9
1,3,5-tri-O-Acetyl-2-deoxy-D-erythro-pentofuranose
Purity:
≥ 98% (HPLC)
Synonym(s):
1,3,5-tri-O-Acetyl-2-deoxy-D-ribose
Documents
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Product Information

1,3,5-tri-O-Acetyl-2-deoxy-D-erythro-pentofuranose is a versatile compound widely utilized in carbohydrate chemistry and pharmaceutical research. This acetylated sugar derivative is particularly valuable for synthesizing nucleoside analogs and other glycosylated compounds, making it an essential building block in the development of antiviral and anticancer agents. Its unique structure enhances solubility and stability, which are critical factors in drug formulation and delivery. Researchers appreciate its role in facilitating glycosylation reactions, allowing for the efficient construction of complex carbohydrate structures.

The compound's ability to serve as a protective group in synthetic pathways further underscores its importance in organic synthesis. Its application extends to the food and cosmetic industries, where it can be used as a flavoring agent or a stabilizer. With its favorable properties and broad applicability, 1,3,5-tri-O-Acetyl-2-deoxy-D-erythro-pentofuranose stands out as a key reagent for professionals seeking to innovate in various fields, from pharmaceuticals to food science.

Synonyms
1,3,5-tri-O-Acetyl-2-deoxy-D-ribose
CAS Number
4594-52-9
Purity
≥ 98% (HPLC)
Molecular Formula
C11H16O7
Molecular Weight
260.24
MDL Number
MFCD08458437
PubChem ID
283455
Appearance
Yellowish brown syrup or white powder
Conditions
Store at 0-8 °C
General Information
Synonyms
1,3,5-tri-O-Acetyl-2-deoxy-D-ribose
CAS Number
4594-52-9
Purity
≥ 98% (HPLC)
Molecular Formula
C11H16O7
Molecular Weight
260.24
MDL Number
MFCD08458437
PubChem ID
283455
Appearance
Yellowish brown syrup or white powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,3,5-tri-O-Acetyl-2-deoxy-D-erythro-pentofuranose is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of nucleoside analogs, which are crucial for developing antiviral and anticancer drugs.
  • Biochemical Research: It is used in studies involving carbohydrate chemistry, helping researchers understand glycosylation processes and enzyme interactions.
  • Drug Delivery Systems: Its acetylated form enhances solubility and stability, making it valuable in formulating drug delivery systems that require controlled release.
  • Diagnostic Applications: The compound can be utilized in the preparation of specific reagents for diagnostic tests, particularly in detecting viral infections.
  • Material Science: It finds applications in the development of biocompatible materials, contributing to advancements in tissue engineering and regenerative medicine.

Citations