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

≥98%,≥99% e.e.

Reagent Code: #59704
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CAS Number 167171-03-1

science Other reagents with same CAS 167171-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 407.4 g/mol
Formula C₂₇H₂₂NOP
thermostat Physical Properties
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 chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of optically active compounds in pharmaceuticals and fine chemicals. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations where high enantiomeric purity is required. The compound's effectiveness stems from its ability to coordinate with metal centers and induce chirality, making it valuable in the development of drugs, agrochemicals, and advanced materials.

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Test Parameter Specification
Appearance White powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,880.00
inventory 250mg
10-20 days ฿5,820.00

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(4R)-2-[2-(Diphenylphosphino)phenyl]-4,5-dihydro-4-phenyloxazole
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of optically active compounds in pharmaceuticals and fine chemicals. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations where high enantiomeric purity is required. The compound's effectiveness stems from its ability to coordinate with metal center

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective synthesis, enabling the production of optically active compounds in pharmaceuticals and fine chemicals. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations where high enantiomeric purity is required. The compound's effectiveness stems from its ability to coordinate with metal centers and induce chirality, making it valuable in the development of drugs, agrochemicals, and advanced materials.

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