1,2,4,6-Tetra-O-acetyl-3-O-allyl-β-D-glucopyranose

≥98%

Reagent Code: #103614
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CAS Number 39698-00-5

science Other reagents with same CAS 39698-00-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.37 g/mol
Formula C₁₇H₂₄O₁₀
thermostat Physical Properties
Melting Point 117-121°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex carbohydrate derivatives. It serves as a key building block in the development of glycosides, which are important in the study of glycobiology and the synthesis of bioactive molecules. Its acetyl and allyl groups provide protection for specific hydroxyl sites, allowing selective reactions to occur during the synthesis process. This compound is also utilized in the production of glycoconjugates, which have applications in drug development, vaccine design, and the study of cellular communication. Additionally, it plays a role in the creation of modified sugars for use in research on enzyme mechanisms and metabolic pathways.

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Test Parameter Specification
Appearance White - Almost White Crystal - Powder
Purity (%) 97.5-100%
Specific Rotation [α]20/D (C=1, CHCl3) -4.0 to -1.0
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,221.00

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1,2,4,6-Tetra-O-acetyl-3-O-allyl-β-D-glucopyranose
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This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex carbohydrate derivatives. It serves as a key building block in the development of glycosides, which are important in the study of glycobiology and the synthesis of bioactive molecules. Its acetyl and allyl groups provide protection for specific hydroxyl sites, allowing selective reactions to occur during the synthesis process. This compound is also utilized in the production of glycoconjugates, whi

This chemical is primarily used in organic synthesis as an intermediate for the preparation of more complex carbohydrate derivatives. It serves as a key building block in the development of glycosides, which are important in the study of glycobiology and the synthesis of bioactive molecules. Its acetyl and allyl groups provide protection for specific hydroxyl sites, allowing selective reactions to occur during the synthesis process. This compound is also utilized in the production of glycoconjugates, which have applications in drug development, vaccine design, and the study of cellular communication. Additionally, it plays a role in the creation of modified sugars for use in research on enzyme mechanisms and metabolic pathways.

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