R-4-Benzyl-2-oxazolidinone

98%

Reagent Code: #229829
label
Alias (R)-4-benzyl-2-oxazolidinone
fingerprint
CAS Number 102029-44-7

science Other reagents with same CAS 102029-44-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.2 g/mol
Formula C₁₀H₁₁NO₂
badge Registry Numbers
MDL Number MFCD00010846
thermostat Physical Properties
Melting Point 88-90 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. It is particularly effective in alkylation and aldol reactions, where it controls stereochemistry and enhances selectivity. After serving its role in directing the stereochemical outcome, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely employed in the synthesis of pharmaceuticals and natural products requiring precise stereocontrol.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿380.00
inventory 25g
10-20 days ฿1,140.00
inventory 100g
10-20 days ฿4,540.00
inventory 2.5kg
10-20 days ฿68,210.00
inventory 500g
10-20 days ฿18,740.00
R-4-Benzyl-2-oxazolidinone
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Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. It is particularly effective in alkylation and aldol reactions, where it controls stereochemistry and enhances selectivity. After serving its role in directing the stereochemical outcome, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely employed in the synthesis of pharmaceuticals and natural products requiring precise stereocontrol.

Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically pure compounds. It is particularly effective in alkylation and aldol reactions, where it controls stereochemistry and enhances selectivity. After serving its role in directing the stereochemical outcome, it can be cleaved under mild conditions, leaving the desired chiral product intact. Widely employed in the synthesis of pharmaceuticals and natural products requiring precise stereocontrol.

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