(R)-N-Boc-2,2-dimethyl-4-vinyloxazolidine

95%

Reagent Code: #37749
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CAS Number 115378-31-9

science Other reagents with same CAS 115378-31-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.3000 g/mol
Formula C₁₂H₂₁NO₃
badge Registry Numbers
MDL Number MFCD18074306
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is widely utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure, featuring a protected amine group (Boc) and a vinyl group, makes it valuable for asymmetric synthesis and stereoselective reactions. It is often employed in the synthesis of complex natural products and chiral intermediates, where the oxazolidine ring serves as a key scaffold for introducing stereochemistry. The vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it versatile in medicinal chemistry and materials science. Additionally, its stability under various reaction conditions makes it a preferred choice for multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,560.00
inventory 250mg
10-20 days ฿15,780.00
inventory 1g
10-20 days ฿36,160.00

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(R)-N-Boc-2,2-dimethyl-4-vinyloxazolidine
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This compound is widely utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure, featuring a protected amine group (Boc) and a vinyl group, makes it valuable for asymmetric synthesis and stereoselective reactions. It is often employed in the synthesis of complex natural products and chiral intermediates, where the oxazolidine ring serves as a key scaffold for introducing stereochemistry. The vinyl group allows for

This compound is widely utilized in organic synthesis as a chiral building block, particularly in the preparation of pharmaceuticals and bioactive molecules. Its structure, featuring a protected amine group (Boc) and a vinyl group, makes it valuable for asymmetric synthesis and stereoselective reactions. It is often employed in the synthesis of complex natural products and chiral intermediates, where the oxazolidine ring serves as a key scaffold for introducing stereochemistry. The vinyl group allows for further functionalization through reactions such as cross-coupling or polymerization, making it versatile in medicinal chemistry and materials science. Additionally, its stability under various reaction conditions makes it a preferred choice for multi-step synthetic processes.

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