3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-α-D-glucopyranosyl Azide

≥98%

Reagent Code: #103701
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CAS Number 102816-25-1

science Other reagents with same CAS 102816-25-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 460.12 g/mol
Formula C₂₀H₂₀N₄O₉
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in carbohydrate chemistry for the synthesis of complex oligosaccharides and glycoconjugates. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for glycosylation reactions. The azide group allows for further functionalization through click chemistry, enabling the attachment of various biomolecules. This compound is particularly valuable in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its acetyl and phthalimido protecting groups ensure selective reactivity, making it a versatile tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,800.00
inventory 25mg
10-20 days ฿3,240.00

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3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-α-D-glucopyranosyl Azide
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Used in carbohydrate chemistry for the synthesis of complex oligosaccharides and glycoconjugates. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for glycosylation reactions. The azide group allows for further functionalization through click chemistry, enabling the attachment of various biomolecules. This compound is particularly valuable in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its

Used in carbohydrate chemistry for the synthesis of complex oligosaccharides and glycoconjugates. It serves as a key intermediate in the preparation of glycosyl donors, which are essential for glycosylation reactions. The azide group allows for further functionalization through click chemistry, enabling the attachment of various biomolecules. This compound is particularly valuable in the development of glycopeptides and glycoproteins, which have applications in drug discovery and vaccine development. Its acetyl and phthalimido protecting groups ensure selective reactivity, making it a versatile tool in organic synthesis.

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