1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-alpha-D-mannopyranose

95%

Reagent Code: #103633
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CAS Number 65556-30-1

science Other reagents with same CAS 65556-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 534.61 g/mol
Formula C₃₁H₃₄O₈
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of oligosaccharides, which are essential for studying biological processes such as cell-cell recognition and signaling. The compound is particularly valuable in glycosylation reactions, where its acetyl and benzyl protecting groups allow for selective manipulation of the sugar molecule. This selectivity is crucial for constructing specific glycosidic linkages in the synthesis of natural products and potential therapeutic agents. Additionally, it is employed in the development of glycoconjugate vaccines, where precise carbohydrate structures are required to elicit targeted immune responses. Its stability and reactivity make it a preferred choice in carbohydrate chemistry research and pharmaceutical applications.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿3,600.00

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1,6-Di-O-acetyl-2,3,4-tri-O-benzyl-alpha-D-mannopyranose
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This chemical is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of oligosaccharides, which are essential for studying biological processes such as cell-cell recognition and signaling. The compound is particularly valuable in glycosylation reactions, where its acetyl and benzyl protecting groups allow for selective manipulation of the sugar molecule. This selectivity is crucial for constructing specific glycosidic linkages in t

This chemical is widely used in the synthesis of complex carbohydrates and glycoconjugates. It serves as a key intermediate in the preparation of oligosaccharides, which are essential for studying biological processes such as cell-cell recognition and signaling. The compound is particularly valuable in glycosylation reactions, where its acetyl and benzyl protecting groups allow for selective manipulation of the sugar molecule. This selectivity is crucial for constructing specific glycosidic linkages in the synthesis of natural products and potential therapeutic agents. Additionally, it is employed in the development of glycoconjugate vaccines, where precise carbohydrate structures are required to elicit targeted immune responses. Its stability and reactivity make it a preferred choice in carbohydrate chemistry research and pharmaceutical applications.

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