S-4-Benzyl-2-oxazolidinone

98%

Reagent Code: #234224
label
Alias (S)-4-benzyl-2-oxazolidinone
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CAS Number 90719-32-7

science Other reagents with same CAS 90719-32-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.2 g/mol
Formula C₁₀H₁₁NO₂
badge Registry Numbers
MDL Number MFCD00064496
thermostat Physical Properties
Melting Point 86-88 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereocenters in complex organic molecules. Its structure facilitates high enantioselectivity in alkylation and aldol reactions, making it valuable in the synthesis of pharmaceuticals and fine chemicals. The auxiliary is easily introduced and removed without racemization, allowing for efficient recovery and reuse in multi-step synthetic routes. Commonly applied in the preparation of beta-amino alcohols and other bioactive intermediates.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 87-91°C
Purity (HPLC) 97.5-100%
Specific Rotation [α]20/D (c=1, CHCl3) -66 to -62°
Purity (GC) 97.5-100%
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure
Solubility C=1 in CHCl3, Clear

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿290.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿350.00
inventory 100g
10-20 days ฿1,100.00
inventory 500g
10-20 days ฿5,350.00

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S-4-Benzyl-2-oxazolidinone
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Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereocenters in complex organic molecules. Its structure facilitates high enantioselectivity in alkylation and aldol reactions, making it valuable in the synthesis of pharmaceuticals and fine chemicals. The auxiliary is easily introduced and removed without racemization, allowing for efficient recovery and reuse in multi-step synthetic routes. Commonly applied in the preparation of beta-amino alcohols and other bioac

Used as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of stereocenters in complex organic molecules. Its structure facilitates high enantioselectivity in alkylation and aldol reactions, making it valuable in the synthesis of pharmaceuticals and fine chemicals. The auxiliary is easily introduced and removed without racemization, allowing for efficient recovery and reuse in multi-step synthetic routes. Commonly applied in the preparation of beta-amino alcohols and other bioactive intermediates.

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