3-Isopropyloxazolidin-2-one

97%

Reagent Code: #198658
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CAS Number 40482-44-8

science Other reagents with same CAS 40482-44-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.16 g/mol
Formula C₆H₁₁NO₂
badge Registry Numbers
MDL Number MFCD16294204
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. It is particularly valuable in the pharmaceutical industry for the synthesis of optically active drugs. The compound helps control stereochemistry during key bond-forming reactions, improving selectivity and yield in complex organic transformations. Its structural rigidity and ability to form stable intermediates make it suitable for use in multi-step synthetic routes, especially in the preparation of beta-amino alcohols and related bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,360.00
inventory 250mg
10-20 days ฿17,560.00
inventory 1g
10-20 days ฿47,310.00
3-Isopropyloxazolidin-2-one
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Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. It is particularly valuable in the pharmaceutical industry for the synthesis of optically active drugs. The compound helps control stereochemistry during key bond-forming reactions, improving selectivity and yield in complex organic transformations. Its structural rigidity and ability to form stable intermediates make it suitable for use in multi-step synthetic routes, especially in the preparation
Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. It is particularly valuable in the pharmaceutical industry for the synthesis of optically active drugs. The compound helps control stereochemistry during key bond-forming reactions, improving selectivity and yield in complex organic transformations. Its structural rigidity and ability to form stable intermediates make it suitable for use in multi-step synthetic routes, especially in the preparation of beta-amino alcohols and related bioactive molecules.
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