4-Phenyloxazolidin-2-one

95%

Reagent Code: #226609
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CAS Number 7480-32-2

science Other reagents with same CAS 7480-32-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.17 g/mol
Formula C₉H₉NO₂
badge Registry Numbers
MDL Number MFCD00601044
thermostat Physical Properties
Melting Point 136.8-137.8 °C
Boiling Point 407°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of stereoselective carbon-carbon and carbon-heteroatom bonds. It is particularly valuable in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. The compound helps control the spatial arrangement of atoms during reactions, improving yield and selectivity. Commonly employed in alkylation, aldol, and Diels-Alder reactions, it can be recycled after the reaction, making it efficient for industrial applications. Also utilized in the development of bioactive molecules and natural product synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿168.00
5g
10-20 days ฿495.00
25g
10-20 days ฿2,442.00
100g
10-20 days ฿17,690.00
4-Phenyloxazolidin-2-one
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Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of stereoselective carbon-carbon and carbon-heteroatom bonds. It is particularly valuable in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. The compound helps control the spatial arrangement of atoms during reactions, improving yield and selectivity. Commonly employed in alkylation, aldol, and Diels-Alder reactions, it can be recycled after the reaction, making it efficient for industrial applications

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of stereoselective carbon-carbon and carbon-heteroatom bonds. It is particularly valuable in the preparation of enantiomerically pure pharmaceuticals and fine chemicals. The compound helps control the spatial arrangement of atoms during reactions, improving yield and selectivity. Commonly employed in alkylation, aldol, and Diels-Alder reactions, it can be recycled after the reaction, making it efficient for industrial applications. Also utilized in the development of bioactive molecules and natural product synthesis.

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