(2R,3R,5S,6S)-5,6-Bis(hydroxymethyl)-2,3-dimethoxy-2,3-dimethyl-1,4-dioxane

98%

Reagent Code: #230311
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CAS Number 173371-55-6

science Other reagents with same CAS 173371-55-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.26 g/mol
Formula C₁₀H₂₀O₆
thermostat Physical Properties
Melting Point 121°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its rigid dioxane backbone with defined stereochemistry makes it valuable for asymmetric synthesis and as a scaffold in drug design. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic sugar-like structures and stabilize bioactive conformations. Also utilized in the preparation of chiral ligands and catalysts for enantioselective transformations.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,250.00
(2R,3R,5S,6S)-5,6-Bis(hydroxymethyl)-2,3-dimethoxy-2,3-dimethyl-1,4-dioxane
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Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its rigid dioxane backbone with defined stereochemistry makes it valuable for asymmetric synthesis and as a scaffold in drug design. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic sugar-like structures and stabilize bioactive conformations. Also utilized in the preparation of chiral ligands and catalysts for enan

Used as a chiral building block in the synthesis of complex organic molecules, particularly in pharmaceuticals and natural products. Its rigid dioxane backbone with defined stereochemistry makes it valuable for asymmetric synthesis and as a scaffold in drug design. Commonly employed in the development of protease inhibitors and antiviral agents due to its ability to mimic sugar-like structures and stabilize bioactive conformations. Also utilized in the preparation of chiral ligands and catalysts for enantioselective transformations.

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