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Catalog Number:
28164
CAS Number:
4451-35-8
Chlorure de 2,3,4,6-tétra-o-acétyl-α-D-glucopyranosyle
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Product Information

2,3,4,6-Tetra-o-acetyl-a-D-glucopyranosyl chloride is a versatile chemical compound widely utilized in the synthesis of glycosides and oligosaccharides. This compound serves as an essential building block in carbohydrate chemistry, enabling researchers to create complex sugar derivatives that are crucial in various fields, including pharmaceuticals, biochemistry, and materials science. Its unique structure, featuring multiple acetyl groups, enhances its reactivity and stability, making it an ideal candidate for glycosylation reactions.

In the pharmaceutical industry, 2,3,4,6-Tetra-o-acetyl-a-D-glucopyranosyl chloride is employed to develop glycosylated drugs, which can improve bioavailability and therapeutic efficacy. Additionally, its application in the synthesis of glycoproteins and glycolipids is significant for research in cell signaling and immunology. Researchers appreciate its efficiency in facilitating the formation of glycosidic bonds, which is pivotal in creating novel compounds with tailored properties. This compound stands out due to its ability to simplify complex synthesis pathways, ultimately saving time and resources in laboratory settings.

CAS Number
4451-35-8
Molecular Formula
C 14 H 19 ClO 9
Molecular Weight
366.75
MDL Number
MFCD00190701
PubChem ID
4207230
Conditions
Conserver à 0-8°C
General Information
CAS Number
4451-35-8
Molecular Formula
C 14 H 19 ClO 9
Molecular Weight
366.75
MDL Number
MFCD00190701
PubChem ID
4207230
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,3,4,6-Tetra-o-acetyl-a-D-glucopyranosyl chloride is widely utilized in research focused on:

  • Synthesis of Glycosides: This compound serves as a key intermediate in the synthesis of various glycosides, which are important in pharmaceuticals and biochemistry for their biological activity.
  • Drug Development: It plays a crucial role in the development of carbohydrate-based drugs, enhancing bioavailability and targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Bioconjugation: The chemical is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Research in Carbohydrate Chemistry: It is extensively used in carbohydrate chemistry research to explore the structure-function relationships of sugars, aiding in the understanding of various biological processes.
  • Food Industry Applications: This compound can be utilized in food chemistry for modifying polysaccharides, improving texture and stability in food products, thus enhancing consumer experience.

Citations