2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate

98%

Reagent Code: #103661
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Alias 2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidic acid
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CAS Number 74808-09-6

science Other reagents with same CAS 74808-09-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 685 g/mol
Formula C₃₆H₃₆Cl₃NO₆
badge Registry Numbers
MDL Number MFCD03427010
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a glycosyl donor in carbohydrate chemistry. It plays a crucial role in the formation of glycosidic bonds, enabling the construction of complex oligosaccharides and glycoconjugates. Its application is particularly significant in the synthesis of biologically active molecules, such as glycoproteins, glycolipids, and other glycosylated natural products. The trichloroacetimidate group enhances reactivity, making it a preferred choice for stereoselective glycosylation reactions. It is widely employed in pharmaceutical research for the development of carbohydrate-based drugs and vaccines, as well as in biochemical studies to investigate glycosylation processes and their biological functions.

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Test Parameter Specification
Appearance White Crystalline Powder
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure

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inventory 1g
10-20 days ฿9,200.00

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2,3,4,6-Tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate
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This chemical is primarily utilized in organic synthesis as a glycosyl donor in carbohydrate chemistry. It plays a crucial role in the formation of glycosidic bonds, enabling the construction of complex oligosaccharides and glycoconjugates. Its application is particularly significant in the synthesis of biologically active molecules, such as glycoproteins, glycolipids, and other glycosylated natural products. The trichloroacetimidate group enhances reactivity, making it a preferred choice for stereoselective glycosylation reactions. It is widely employed in pharmaceutical research for the development of carbohydrate-based drugs and vaccines, as well as in biochemical studies to investigate glycosylation processes and their biological functions.
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