2,3,4,6-Tetra-O-benzyl-D-glucopyranosyl Fluoride

≥96%

Reagent Code: #103658
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CAS Number 122741-44-0

science Other reagents with same CAS 122741-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.65 g/mol
Formula C₃₄H₃₅FO₅
badge Registry Numbers
MDL Number MFCD01862264
thermostat Physical Properties
Melting Point 42-47°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis as a glycosyl donor in the formation of glycosidic bonds. It is particularly valuable in carbohydrate chemistry for constructing complex oligosaccharides and glycoconjugates. Its benzyl-protected groups ensure stability during reactions, while the fluoride moiety acts as a good leaving group, facilitating efficient glycosylation processes. This compound is often employed in the development of pharmaceuticals, especially in the synthesis of glycosylated natural products and bioactive molecules. Additionally, it plays a role in research focused on understanding enzymatic glycosylation mechanisms and designing glycosidase inhibitors.

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inventory 100mg
10-20 days ฿2,241.00

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2,3,4,6-Tetra-O-benzyl-D-glucopyranosyl Fluoride
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This chemical is primarily used in organic synthesis as a glycosyl donor in the formation of glycosidic bonds. It is particularly valuable in carbohydrate chemistry for constructing complex oligosaccharides and glycoconjugates. Its benzyl-protected groups ensure stability during reactions, while the fluoride moiety acts as a good leaving group, facilitating efficient glycosylation processes. This compound is often employed in the development of pharmaceuticals, especially in the synthesis of glycosylated

This chemical is primarily used in organic synthesis as a glycosyl donor in the formation of glycosidic bonds. It is particularly valuable in carbohydrate chemistry for constructing complex oligosaccharides and glycoconjugates. Its benzyl-protected groups ensure stability during reactions, while the fluoride moiety acts as a good leaving group, facilitating efficient glycosylation processes. This compound is often employed in the development of pharmaceuticals, especially in the synthesis of glycosylated natural products and bioactive molecules. Additionally, it plays a role in research focused on understanding enzymatic glycosylation mechanisms and designing glycosidase inhibitors.

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