2-((S)-4-Phenyl-4,5-dihydrooxazol-2-yl)-2-((S)-4-phenyloxazolidin-2-ylidene)acetonitrile

97%

Reagent Code: #235853
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CAS Number 150639-33-1

science Other reagents with same CAS 150639-33-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.3679 g/mol
Formula C₂₀H₁₇N₃O₂
badge Registry Numbers
MDL Number MFCD00192394
thermostat Physical Properties
Melting Point 146-148 °C(lit.)
Boiling Point 457.5 °C at 760mmHg
inventory_2 Storage & Handling
Density 1.27 g/cm3
Storage 2-8°C

description Product Description

Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. It plays a key role in facilitating carbon-carbon bond-forming reactions, such as aldol or Michael additions, where high enantioselectivity is required. Its rigid oxazoline and oxazolidine framework enhances stereocontrol, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products. Commonly employed in transition metal-catalyzed reactions, especially with copper or nickel complexes, to achieve high optical purity in the final product.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
inventory 250mg
10-20 days ฿3,410.00
inventory 1g
10-20 days ฿13,640.00
inventory 5g
10-20 days ฿50,950.00
2-((S)-4-Phenyl-4,5-dihydrooxazol-2-yl)-2-((S)-4-phenyloxazolidin-2-ylidene)acetonitrile
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Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. It plays a key role in facilitating carbon-carbon bond-forming reactions, such as aldol or Michael additions, where high enantioselectivity is required. Its rigid oxazoline and oxazolidine framework enhances stereocontrol, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products. Commonly employed in transition metal-catalyzed reactions, especia

Used as a chiral auxiliary or ligand in asymmetric synthesis, particularly in enantioselective catalysis. It plays a key role in facilitating carbon-carbon bond-forming reactions, such as aldol or Michael additions, where high enantioselectivity is required. Its rigid oxazoline and oxazolidine framework enhances stereocontrol, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and natural products. Commonly employed in transition metal-catalyzed reactions, especially with copper or nickel complexes, to achieve high optical purity in the final product.

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