(4R,5R)-Diethyl 2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylate

98%

Reagent Code: #231696
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CAS Number 59779-75-8

science Other reagents with same CAS 59779-75-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.26 g/mol
Formula C₁₁H₁₈O₆
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of optically active pharmaceuticals and natural products. Its rigid dioxolane ring with defined stereochemistry allows for stereoselective transformations, making it valuable in the synthesis of complex molecules where control of chirality is critical. Commonly employed in the development of enzyme inhibitors and bioactive compounds, it serves as a protected glycerol derivative with two ester functionalities that can be selectively modified. Its stability and ease of handling make it suitable for multi-step synthetic routes in medicinal chemistry and process development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿670.00
inventory 250mg
10-20 days ฿840.00
inventory 5g
10-20 days ฿5,130.00
inventory 1g
10-20 days ฿1,630.00
(4R,5R)-Diethyl 2,2-Dimethyl-1,3-Dioxolane-4,5-Dicarboxylate
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Used as a chiral building block in asymmetric synthesis, particularly in the preparation of optically active pharmaceuticals and natural products. Its rigid dioxolane ring with defined stereochemistry allows for stereoselective transformations, making it valuable in the synthesis of complex molecules where control of chirality is critical. Commonly employed in the development of enzyme inhibitors and bioactive compounds, it serves as a protected glycerol derivative with two ester functionalities that can

Used as a chiral building block in asymmetric synthesis, particularly in the preparation of optically active pharmaceuticals and natural products. Its rigid dioxolane ring with defined stereochemistry allows for stereoselective transformations, making it valuable in the synthesis of complex molecules where control of chirality is critical. Commonly employed in the development of enzyme inhibitors and bioactive compounds, it serves as a protected glycerol derivative with two ester functionalities that can be selectively modified. Its stability and ease of handling make it suitable for multi-step synthetic routes in medicinal chemistry and process development.

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