2,3,4,6-Tetra-O-benzoyl-D-mannopyranose

≥93%

Reagent Code: #103666
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CAS Number 113544-59-5

science Other reagents with same CAS 113544-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 596.59 g/mol
Formula C₃₄H₂₈O₁₀
badge Registry Numbers
MDL Number MFCD02683399
thermostat Physical Properties
Melting Point 179-185°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily used in organic synthesis as a protected form of D-mannose. It serves as a key intermediate in the production of complex carbohydrates and glycoconjugates, which are essential in biochemical research and pharmaceutical development. The benzoyl groups provide stability during chemical reactions, allowing for selective manipulation of the sugar moiety. It is particularly valuable in the synthesis of oligosaccharides, glycoproteins, and other biologically active molecules. Additionally, it finds application in the preparation of glycosyl donors for glycosylation reactions, which are crucial in creating natural products and therapeutic agents. Its role in carbohydrate chemistry makes it a vital tool for advancing studies in glycoscience and drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,364.00
inventory 200mg
10-20 days ฿2,133.00

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2,3,4,6-Tetra-O-benzoyl-D-mannopyranose
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This chemical is primarily used in organic synthesis as a protected form of D-mannose. It serves as a key intermediate in the production of complex carbohydrates and glycoconjugates, which are essential in biochemical research and pharmaceutical development. The benzoyl groups provide stability during chemical reactions, allowing for selective manipulation of the sugar moiety. It is particularly valuable in the synthesis of oligosaccharides, glycoproteins, and other biologically active molecules. Additio

This chemical is primarily used in organic synthesis as a protected form of D-mannose. It serves as a key intermediate in the production of complex carbohydrates and glycoconjugates, which are essential in biochemical research and pharmaceutical development. The benzoyl groups provide stability during chemical reactions, allowing for selective manipulation of the sugar moiety. It is particularly valuable in the synthesis of oligosaccharides, glycoproteins, and other biologically active molecules. Additionally, it finds application in the preparation of glycosyl donors for glycosylation reactions, which are crucial in creating natural products and therapeutic agents. Its role in carbohydrate chemistry makes it a vital tool for advancing studies in glycoscience and drug discovery.

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