(S)-4-Benzyl-2-(quinolin-2-yl)-4,5-dihydrooxazole

98%, ee 99%

Reagent Code: #38541
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CAS Number 1252576-14-9

science Other reagents with same CAS 1252576-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.34314 g/mol
Formula C₁₉H₁₆N₂O
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its structure, featuring a quinoline moiety and a dihydrooxazole ring, makes it effective in coordinating with transition metals, enhancing the efficiency and selectivity of catalytic processes. It is commonly applied in pharmaceutical research for the synthesis of chiral drugs, where achieving high enantiomeric purity is crucial. Additionally, it is used in organic synthesis to produce complex molecules with specific stereochemical configurations, aiding in the development of advanced materials and fine chemicals.

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Test Parameter Specification
Appearance White to Light Yellow to Yellow Solid
Purity (%) 97.5-100%
Enantiomeric Excess (%) 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5 mg
10-20 days ฿310.00
inventory 1 g
10-20 days ฿13,200.00
inventory 25 mg
10-20 days ฿780.00
inventory 100 mg
10-20 days ฿1,440.00
inventory 250 mg
10-20 days ฿3,470.00

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(S)-4-Benzyl-2-(quinolin-2-yl)-4,5-dihydrooxazole
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This compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its structure, featuring a quinoline moiety and a dihydrooxazole ring, makes it effective in coordinating with transition metals, enhancing the efficiency and selectivity of catalytic processes. It is commonly applied in pharmaceutical research for the syn

This compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. It plays a significant role in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. Its structure, featuring a quinoline moiety and a dihydrooxazole ring, makes it effective in coordinating with transition metals, enhancing the efficiency and selectivity of catalytic processes. It is commonly applied in pharmaceutical research for the synthesis of chiral drugs, where achieving high enantiomeric purity is crucial. Additionally, it is used in organic synthesis to produce complex molecules with specific stereochemical configurations, aiding in the development of advanced materials and fine chemicals.

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