(S)-(-)-4-Isopropyl-2-oxazolidinone

98%

Reagent Code: #234266
label
Alias (S)-4-isopropyl-2-oxazolidinone
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CAS Number 17016-83-0

science Other reagents with same CAS 17016-83-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.16 g/mol
Formula C₆H₁₁NO₂
badge Registry Numbers
MDL Number MFCD00010847
thermostat Physical Properties
Melting Point 70-73 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereocenters in complex organic molecules. It is particularly effective in enantioselective alkylation and aldol reactions, where it controls the spatial arrangement of atoms during bond formation. Its rigid cyclic structure and ability to coordinate with metal ions enhance stereoselectivity. After serving its purpose, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely applied in the synthesis of pharmaceuticals and natural products requiring high optical purity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿450.00
inventory 25g
10-20 days ฿2,160.00
inventory 100g
10-20 days ฿8,550.00
inventory 500g
10-20 days ฿40,050.00
(S)-(-)-4-Isopropyl-2-oxazolidinone
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Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereocenters in complex organic molecules. It is particularly effective in enantioselective alkylation and aldol reactions, where it controls the spatial arrangement of atoms during bond formation. Its rigid cyclic structure and ability to coordinate with metal ions enhance stereoselectivity. After serving its purpose, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely applied

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereocenters in complex organic molecules. It is particularly effective in enantioselective alkylation and aldol reactions, where it controls the spatial arrangement of atoms during bond formation. Its rigid cyclic structure and ability to coordinate with metal ions enhance stereoselectivity. After serving its purpose, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely applied in the synthesis of pharmaceuticals and natural products requiring high optical purity.

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