2,3,4-Tri-O-acetyl-a-D-glucuronide methyl ester trichloroacetimidate

98%

Reagent Code: #66409
label
Alias 3,4,6-tri-o-acetyl-ALPHA-D-glucopyranose 1,2-(methyl orthoate); 3,4,6-tri-oxo-acetyl-α-D-glucopyranose 1 ,2-(Methyl orthoacetate)
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CAS Number 92420-89-8

science Other reagents with same CAS 92420-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 478.66 g/mol
Formula C₁₅H₁₈Cl₃NO₁₀
badge Registry Numbers
MDL Number MFCD02094293
inventory_2 Storage & Handling
Storage -20°C, stored in inert gas

description Product Description

This compound is primarily utilized in synthetic organic chemistry as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its trichloroacetimidate group makes it a highly reactive glycosyl donor, enabling efficient glycosylation reactions under mild conditions. This is particularly valuable in the synthesis of glycoconjugates, which are essential in the development of pharmaceuticals, vaccines, and biochemical probes. Additionally, its acetyl-protected glucuronide moiety allows for selective deprotection, facilitating the construction of diverse carbohydrate structures. This compound is also employed in the study of enzymatic processes and the development of glycosidase inhibitors, which have potential therapeutic applications in treating metabolic disorders and infections.

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Test Parameter Specification
Appearance White Powder
Purity 97.5-100
Composition Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,130.00
inventory 1g
10-20 days ฿9,290.00

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2,3,4-Tri-O-acetyl-a-D-glucuronide methyl ester trichloroacetimidate
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This compound is primarily utilized in synthetic organic chemistry as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its trichloroacetimidate group makes it a highly reactive glycosyl donor, enabling efficient glycosylation reactions under mild conditions. This is particularly valuable in the synthesis of glycoconjugates, which are essential in the development of pharmaceuticals, vaccines, and biochemical probes. Additionally, its acetyl-protected glucuronide moiety al

This compound is primarily utilized in synthetic organic chemistry as a key intermediate for the preparation of complex glycosides and oligosaccharides. Its trichloroacetimidate group makes it a highly reactive glycosyl donor, enabling efficient glycosylation reactions under mild conditions. This is particularly valuable in the synthesis of glycoconjugates, which are essential in the development of pharmaceuticals, vaccines, and biochemical probes. Additionally, its acetyl-protected glucuronide moiety allows for selective deprotection, facilitating the construction of diverse carbohydrate structures. This compound is also employed in the study of enzymatic processes and the development of glycosidase inhibitors, which have potential therapeutic applications in treating metabolic disorders and infections.

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