Benzyl (2R,4R)-5-oxo-2,4-diphenyloxazolidine-3-carboxylate

98%

Reagent Code: #229388
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CAS Number 205654-83-7

science Other reagents with same CAS 205654-83-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.4 g/mol
Formula C₂₃H₁₉NO₄
badge Registry Numbers
MDL Number MFCD32644135
thermostat Physical Properties
Boiling Point 591.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.270±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective alkylation and aldol reactions. Its rigid oxazolidine ring structure helps control stereochemistry, enabling high diastereoselectivity. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including active pharmaceutical ingredients (APIs) where stereo purity is critical. After serving its purpose, the auxiliary can be cleaved under mild conditions, leaving the desired chiral product intact. Also utilized in the development of chiral ligands and catalysts for transition-metal-mediated reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,730.00
inventory 250mg
10-20 days ฿19,940.00
Benzyl (2R,4R)-5-oxo-2,4-diphenyloxazolidine-3-carboxylate
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Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective alkylation and aldol reactions. Its rigid oxazolidine ring structure helps control stereochemistry, enabling high diastereoselectivity. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including active pharmaceutical ingredients (APIs) where stereo purity is critical. After serving its purpose, the auxiliary can be cleaved under mild conditions, leaving the desired chiral

Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective alkylation and aldol reactions. Its rigid oxazolidine ring structure helps control stereochemistry, enabling high diastereoselectivity. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including active pharmaceutical ingredients (APIs) where stereo purity is critical. After serving its purpose, the auxiliary can be cleaved under mild conditions, leaving the desired chiral product intact. Also utilized in the development of chiral ligands and catalysts for transition-metal-mediated reactions.

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