3,5,6-Tri-O-benzyl-1,2-O-Isopropylidene-α-D-glucofuranose

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Reagent Code: #103707
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CAS Number 53928-30-6

science Other reagents with same CAS 53928-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 490.58736 g/mol
Formula C₃₀H₃₄O₆
badge Registry Numbers
MDL Number MFCD08703754
thermostat Physical Properties
Boiling Point 589.7°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.2 g/ml
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a protected form of glucose, enabling selective reactions at specific hydroxyl groups. It is particularly valuable in carbohydrate chemistry for constructing complex oligosaccharides and glycoconjugates. The benzyl groups provide stability and prevent unwanted side reactions, while the isopropylidene moiety protects the furanose ring. This chemical is instrumental in the development of pharmaceuticals, especially in the synthesis of glycosylated drugs and bioactive molecules. Its application extends to research in glycobiology, where it aids in studying carbohydrate-protein interactions and developing novel therapeutic agents.

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inventory 1g
10-20 days ฿13,160.00
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3,5,6-Tri-O-benzyl-1,2-O-Isopropylidene-α-D-glucofuranose
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Used primarily in organic synthesis, this compound serves as a protected form of glucose, enabling selective reactions at specific hydroxyl groups. It is particularly valuable in carbohydrate chemistry for constructing complex oligosaccharides and glycoconjugates. The benzyl groups provide stability and prevent unwanted side reactions, while the isopropylidene moiety protects the furanose ring. This chemical is instrumental in the development of pharmaceuticals, especially in the synthesis of glycosylate

Used primarily in organic synthesis, this compound serves as a protected form of glucose, enabling selective reactions at specific hydroxyl groups. It is particularly valuable in carbohydrate chemistry for constructing complex oligosaccharides and glycoconjugates. The benzyl groups provide stability and prevent unwanted side reactions, while the isopropylidene moiety protects the furanose ring. This chemical is instrumental in the development of pharmaceuticals, especially in the synthesis of glycosylated drugs and bioactive molecules. Its application extends to research in glycobiology, where it aids in studying carbohydrate-protein interactions and developing novel therapeutic agents.

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