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Catalog Number:
27248
CAS Number:
14218-11-2
Bromuro de 2,3,4,6-tetra -O -benzoil-α-D-glucopiranosilo
Purity:
≥ 98% (ensayo)
Synonym(s):
Tetrabenzoato de bromuro de α-D-glucopiranosilo
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Product Information

2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl bromide is a versatile glycosylating agent widely utilized in organic synthesis and carbohydrate chemistry. This compound serves as a key intermediate in the preparation of various glycosides, which are essential in the development of pharmaceuticals, agrochemicals, and functional materials. Its unique structure, featuring multiple benzoyl groups, enhances its stability and reactivity, making it an ideal choice for researchers looking to create complex carbohydrate structures.

In addition to its applications in synthetic chemistry, 2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl bromide is also employed in the study of glycoproteins and glycolipids, contributing to advancements in biochemistry and molecular biology. Its ability to selectively react with nucleophiles allows for the efficient formation of glycosidic bonds, facilitating the synthesis of biologically relevant compounds. This compound stands out for its high yield and purity, making it a reliable choice for both academic and industrial applications.

Synonyms
Tetrabenzoato de bromuro de α-D-glucopiranosilo
CAS Number
14218-11-2
Purity
≥ 98% (ensayo)
Molecular Formula
C34H27BrO9
Molecular Weight
659.48
MDL Number
MFCD00010694
PubChem ID
3511428
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Tetrabenzoato de bromuro de α-D-glucopiranosilo
CAS Number
14218-11-2
Purity
≥ 98% (ensayo)
Molecular Formula
C34H27BrO9
Molecular Weight
659.48
MDL Number
MFCD00010694
PubChem ID
3511428
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3,4,6-Tetra-O-benzoyl-α-D-glucopyranosyl bromide is widely utilized in research focused on:

  • Synthetic Organic Chemistry: This compound serves as a key intermediate in the synthesis of various glycosides, enabling chemists to create complex carbohydrate structures efficiently.
  • Pharmaceutical Development: It is employed in the design of drug molecules that require glycosylation, enhancing the bioavailability and efficacy of therapeutic agents.
  • Bioconjugation: The compound is used to attach sugars to proteins or other biomolecules, facilitating the study of glycoproteins and their roles in biological processes.
  • Food Industry: It can be utilized in the development of flavoring agents and sweeteners, contributing to the formulation of products with enhanced taste profiles.
  • Research in Glycobiology: This chemical plays a significant role in exploring the structure-function relationships of carbohydrates, aiding in the understanding of their biological significance.

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