(4S)-2-[2-(Diphenylphosphino)phenyl]-4,5-dihydro-4-phenyloxazole

98%

Reagent Code: #59717
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CAS Number 148461-15-8

science Other reagents with same CAS 148461-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 407.4 g/mol
Formula C₂₇H₂₂NOP
thermostat Physical Properties
Melting Point 89-93 °C
Boiling Point 555.7±50.0 °C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is widely used as a ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its chiral structure allows for the production of optically active compounds, which are essential in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the development of novel catalytic systems for organic synthesis, enhancing both efficiency and selectivity in complex reactions.

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Test Parameter Specification
Appearance White to yellow powder or crystals
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿17,200.00
inventory 100mg
10-20 days ฿3,680.00

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(4S)-2-[2-(Diphenylphosphino)phenyl]-4,5-dihydro-4-phenyloxazole
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This chemical is widely used as a ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its chiral structure allows for the production of optically active compounds, which are essential in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the development of novel catalytic syste

This chemical is widely used as a ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cross-coupling reactions. Its chiral structure allows for the production of optically active compounds, which are essential in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the development of novel catalytic systems for organic synthesis, enhancing both efficiency and selectivity in complex reactions.

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