Ethyl 2-Deoxy-2-Phthalimido-1-thio-β-D-thioglucopyranoside

≥98%

Reagent Code: #103881
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CAS Number 130539-43-4

science Other reagents with same CAS 130539-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 353.39 g/mol
Formula C₁₆H₁₉NO₆S
thermostat Physical Properties
Boiling Point 594.3±50.0℃
inventory_2 Storage & Handling
Density 1.52±0.1 g/cm3
Storage 2-8℃

description Product Description

This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of glycosides and glycoconjugates. It serves as a protected form of a glucosamine derivative, enabling selective modification of the sugar moiety in complex molecular structures. Its application is significant in the development of pharmaceuticals, particularly in the synthesis of antibiotics, antiviral agents, and other bioactive molecules. Additionally, it is utilized in research for studying glycosylation reactions and enzyme mechanisms, contributing to advancements in glycobiology and medicinal chemistry.

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Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,380.00
inventory 1g
10-20 days ฿4,980.00

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Ethyl 2-Deoxy-2-Phthalimido-1-thio-β-D-thioglucopyranoside
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This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of glycosides and glycoconjugates. It serves as a protected form of a glucosamine derivative, enabling selective modification of the sugar moiety in complex molecular structures. Its application is significant in the development of pharmaceuticals, particularly in the synthesis of antibiotics, antiviral agents, and other bioactive molecules. Additionally, it is utilized in research fo

This compound is primarily used in organic synthesis and carbohydrate chemistry as a key intermediate for the preparation of glycosides and glycoconjugates. It serves as a protected form of a glucosamine derivative, enabling selective modification of the sugar moiety in complex molecular structures. Its application is significant in the development of pharmaceuticals, particularly in the synthesis of antibiotics, antiviral agents, and other bioactive molecules. Additionally, it is utilized in research for studying glycosylation reactions and enzyme mechanisms, contributing to advancements in glycobiology and medicinal chemistry.

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