((5R,6S,6aR)-6-(benzyloxy)-5-((benzyloxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol

95%

Reagent Code: #84757
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CAS Number 206055-83-6

science Other reagents with same CAS 206055-83-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 400.46 g/mol
Formula C₂₃H₂₈O₆
thermostat Physical Properties
Boiling Point 531.4±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. Its structure, featuring multiple protective groups like benzyloxy and tetrahydrofuro[2,3-d][1,3]dioxol, makes it a valuable intermediate in the preparation of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, where they act by inhibiting the replication of DNA or RNA in target cells. Additionally, the compound's stereochemistry and functional groups allow for precise modifications, enabling researchers to tailor its properties for specific therapeutic applications. Its role in carbohydrate chemistry is also notable, as it aids in the construction of glycosidic linkages, which are essential in the synthesis of oligosaccharides and glycoconjugates used in drug discovery and biochemical studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,190.00
inventory 250mg
10-20 days ฿14,625.00
inventory 1g
10-20 days ฿29,250.00

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((5R,6S,6aR)-6-(benzyloxy)-5-((benzyloxy)methyl)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. Its structure, featuring multiple protective groups like benzyloxy and tetrahydrofuro[2,3-d][1,3]dioxol, makes it a valuable intermediate in the preparation of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, where they act by inhibiting the replication of DNA or RNA in target cells. Additionally, the compound's stereochemi

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the field of medicinal chemistry. Its structure, featuring multiple protective groups like benzyloxy and tetrahydrofuro[2,3-d][1,3]dioxol, makes it a valuable intermediate in the preparation of nucleoside analogs. These analogs are crucial in the development of antiviral and anticancer drugs, where they act by inhibiting the replication of DNA or RNA in target cells. Additionally, the compound's stereochemistry and functional groups allow for precise modifications, enabling researchers to tailor its properties for specific therapeutic applications. Its role in carbohydrate chemistry is also notable, as it aids in the construction of glycosidic linkages, which are essential in the synthesis of oligosaccharides and glycoconjugates used in drug discovery and biochemical studies.

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