(R)-4-(Tert-Butyl)Oxazolidin-2-One

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Reagent Code: #231615
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CAS Number 142618-93-7

science Other reagents with same CAS 142618-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.18 g/mol
Formula C₇H₁₃NO₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereoisomers in pharmaceutical and fine chemical manufacturing. Its rigid structure helps control the stereochemical outcome of reactions, particularly in alkylations, aldol additions, and Diels-Alder reactions. After serving its role, it can be cleaved and recycled, making it efficient for multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients where high enantiomeric purity is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,940.00
inventory 1g
10-20 days ฿11,970.00
inventory 5g
10-20 days ฿53,190.00
inventory 250mg
10-20 days ฿4,880.00
(R)-4-(Tert-Butyl)Oxazolidin-2-One
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Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereoisomers in pharmaceutical and fine chemical manufacturing. Its rigid structure helps control the stereochemical outcome of reactions, particularly in alkylations, aldol additions, and Diels-Alder reactions. After serving its role, it can be cleaved and recycled, making it efficient for multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients where high enantiomeric purity i

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereoisomers in pharmaceutical and fine chemical manufacturing. Its rigid structure helps control the stereochemical outcome of reactions, particularly in alkylations, aldol additions, and Diels-Alder reactions. After serving its role, it can be cleaved and recycled, making it efficient for multi-step synthesis. Commonly employed in the development of active pharmaceutical ingredients where high enantiomeric purity is required.

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