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Catalog Number:
29364
CAS Number:
54423-54-0
2,3,4,6-Tétra- O -benzyl-D-glucose-1- p -nitrobenzoate
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Product Information

2,3,4,6-Tetra-O-benzyl-D-glucose-1-p-nitrobenzoate is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound, characterized by its multiple benzyl ether groups, enhances its solubility and stability, making it an excellent choice for various applications. Its unique structure allows for selective reactions, which are crucial in the synthesis of complex carbohydrates and glycosides. Researchers often leverage its properties to develop new drug formulations and study glycosylation processes, which are vital in biochemistry and medicinal chemistry.

In addition, 2,3,4,6-Tetra-O-benzyl-D-glucose-1-p-nitrobenzoate serves as a valuable intermediate in the preparation of glycosyl donors, facilitating the formation of glycosidic bonds in carbohydrate chemistry. Its ability to protect hydroxyl groups while allowing for specific reactivity makes it a preferred choice among chemists looking to streamline their synthetic pathways. With its robust performance in various chemical reactions, this compound stands out as a reliable tool for both academic and industrial applications.

CAS Number
54423-54-0
Molecular Formula
C 41 H 399
Molecular Weight
689.76
MDL Number
MFCD12407149
PubChem ID
314411
Conditions
Conserver à 0-8°C
General Information
CAS Number
54423-54-0
Molecular Formula
C 41 H 399
Molecular Weight
689.76
MDL Number
MFCD12407149
PubChem ID
314411
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-benzyl-D-glucose-1-p-nitrobenzoate is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of glycosides and other carbohydrate derivatives, enabling chemists to create complex molecules for pharmaceuticals and agrochemicals.
  • Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their solubility and bioavailability, which is crucial in the formulation of effective medications.
  • Biochemical Research: Researchers use this compound to study carbohydrate interactions and enzyme activity, providing insights into metabolic pathways and potential therapeutic targets.
  • Material Science: It can be employed in the development of novel materials with specific properties, such as hydrogels or coatings, which are important in biomedical applications.
  • Analytical Chemistry: The compound is useful in the preparation of standards for chromatographic techniques, aiding in the accurate analysis of carbohydrate content in various samples.

Citations