(S)-4-(tert-Butyl)-2-(2-(diphenylphosphino)phenyl)-4,5-dihydrooxazole

98%, ee 99%

Reagent Code: #37794
fingerprint
CAS Number 148461-16-9

science Other reagents with same CAS 148461-16-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 387.45 g/mol
Formula C₂₅H₂₆NOP
badge Registry Numbers
MDL Number MFCD09998277
thermostat Physical Properties
Melting Point 111-116 °C
Boiling Point 498.9±28.0 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its sterically hindered and electron-rich structure enhances selectivity and efficiency in producing chiral molecules, making it valuable in pharmaceutical synthesis for creating enantiopure drugs. Additionally, it is employed in academic and industrial research to develop new catalytic processes for fine chemical production.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5 mg
10-20 days ฿440.00
inventory 250 mg
10-20 days ฿4,520.00
inventory 100 mg
10-20 days ฿2,300.00
inventory 25 mg
10-20 days ฿1,010.00
inventory 1 g
10-20 days ฿14,510.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-4-(tert-Butyl)-2-(2-(diphenylphosphino)phenyl)-4,5-dihydrooxazole
No image available

This compound is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its sterically hindered and electron-rich structure enhances selectivity and efficiency in producing chiral molecules, making it valuable in pharmaceutical synthesis for creating enantiopure drugs. Additionally, it is employed in

This compound is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its sterically hindered and electron-rich structure enhances selectivity and efficiency in producing chiral molecules, making it valuable in pharmaceutical synthesis for creating enantiopure drugs. Additionally, it is employed in academic and industrial research to develop new catalytic processes for fine chemical production.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...