4-Ethyloxazolidin-2-one

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Reagent Code: #184019
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CAS Number 16112-60-0

science Other reagents with same CAS 16112-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 115.13 g/mol
Formula C₅H₉NO₂
badge Registry Numbers
MDL Number MFCD00068849
thermostat Physical Properties
Boiling Point 119-126 °C
inventory_2 Storage & Handling
Density 1.047±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of stereoselective carbon-carbon bonds. It is particularly valuable in the pharmaceutical industry for the synthesis of optically active intermediates. The compound helps control stereochemistry during reactions such as alkylations, aldol condensations, and Michael additions. After serving its role, it can be cleaved under mild conditions, leaving the desired enantiomerically enriched product. Its stability and ease of introduction make it a preferred choice in complex molecule assembly, including natural products and active pharmaceutical ingredients.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,190.00
inventory 1g
10-20 days ฿3,180.00

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4-Ethyloxazolidin-2-one
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Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of stereoselective carbon-carbon bonds. It is particularly valuable in the pharmaceutical industry for the synthesis of optically active intermediates. The compound helps control stereochemistry during reactions such as alkylations, aldol condensations, and Michael additions. After serving its role, it can be cleaved under mild conditions, leaving the desired enantiomerically enriched product. Its stability and ease of introductio

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of stereoselective carbon-carbon bonds. It is particularly valuable in the pharmaceutical industry for the synthesis of optically active intermediates. The compound helps control stereochemistry during reactions such as alkylations, aldol condensations, and Michael additions. After serving its role, it can be cleaved under mild conditions, leaving the desired enantiomerically enriched product. Its stability and ease of introduction make it a preferred choice in complex molecule assembly, including natural products and active pharmaceutical ingredients.

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