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Catalog Number:
27880
CAS Number:
97614-43-2
2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-a-D-arabinofuranose
Purity:
≥ 98% (HPLC)
Documents
$22.03 /1G
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Product Information

2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-a-D-arabinofuranose is a specialized sugar derivative that plays a significant role in the field of medicinal chemistry and biochemistry. This compound is recognized for its unique structural features, including the presence of a fluorine atom, which enhances its stability and reactivity compared to other sugar analogs. Its tri-O-benzoyl protection makes it particularly valuable in synthetic applications, allowing for selective reactions that are crucial in the development of nucleoside analogs and other pharmaceutical intermediates.

Researchers have utilized this compound in the synthesis of antiviral agents and other therapeutic molecules, demonstrating its potential in drug discovery and development. Its ability to mimic natural sugars while providing enhanced properties makes it an attractive candidate for further exploration in glycoscience and medicinal applications. The compound's versatility and stability position it as a key player in advancing research in carbohydrate chemistry and related fields.

CAS Number
97614-43-2
Purity
≥ 98% (HPLC)
Molecular Formula
C26H21FO7
Molecular Weight
464.44
MDL Number
MFCD00083339
PubChem ID
357685
Melting Point
82-90 ?C
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = +74 ± 2 º (C=1 in CH2Cl2
Conditions
Store at 0-8°C
General Information
CAS Number
97614-43-2
Purity
≥ 98% (HPLC)
Molecular Formula
C26H21FO7
Molecular Weight
464.44
MDL Number
MFCD00083339
PubChem ID
357685
Melting Point
82-90 ?C
Appearance
White to off-white crystalline powder
Optical Rotation
[a]D20 = +74 ± 2 º (C=1 in CH2Cl2
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

2-Deoxy-2-fluoro-1,3,5-tri-O-benzoyl-a-D-arabinofuranose is widely utilized in research focused on:

  • Antiviral Drug Development: This compound serves as a crucial intermediate in synthesizing antiviral agents, particularly those targeting viral replication processes, enhancing the efficacy of treatments for diseases like HIV and hepatitis.
  • Glycosylation Studies: It is employed in glycosylation reactions to create glycosides, which are vital for studying carbohydrate-protein interactions and their biological implications in various fields, including immunology and cell biology.
  • Pharmaceutical Formulations: The compound is used in the formulation of prodrugs, which can improve the bioavailability of active pharmaceutical ingredients, leading to more effective therapies with fewer side effects.
  • Biochemical Research: Researchers utilize it to investigate enzyme mechanisms and substrate specificity, providing insights that can lead to the development of novel enzymes or inhibitors.
  • Material Science: This chemical is also explored in the development of new materials, such as polymers or coatings, that require specific functional groups for enhanced performance in various applications.

Citations