tert-Butyl (3R,4R)-3,4-dimethoxypyrrolidine-1-carboxylate

≥95%

Reagent Code: #84420
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CAS Number 942309-05-9

science Other reagents with same CAS 942309-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.29 g/mol
Formula C₁₁H₂₁NO₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals. Its stereochemistry and functional groups make it valuable for constructing complex molecules with high enantiomeric purity. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, where precise control over stereochemistry is crucial. Additionally, it can serve as a protecting group for amines in multi-step synthetic processes, ensuring selective reactivity and stability during chemical transformations. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,700.00

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tert-Butyl (3R,4R)-3,4-dimethoxypyrrolidine-1-carboxylate
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals. Its stereochemistry and functional groups make it valuable for constructing complex molecules with high enantiomeric purity. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, where precise control over stereochemistry is crucial. Additionally, it can serve as a protecting group for amines in mu

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral building block or intermediate in the production of pharmaceuticals. Its stereochemistry and functional groups make it valuable for constructing complex molecules with high enantiomeric purity. It is often employed in the synthesis of bioactive compounds, including potential drug candidates, where precise control over stereochemistry is crucial. Additionally, it can serve as a protecting group for amines in multi-step synthetic processes, ensuring selective reactivity and stability during chemical transformations. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of new therapeutic agents.

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