R-()-6,6'-Bis(diphenylphosphino)-2,2',3,3'-tetrahydro-5,5'-bi-1,4-benzodioxin

98%

Reagent Code: #68819
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CAS Number 445467-61-8

science Other reagents with same CAS 445467-61-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 638.63 g/mol
Formula C₄₀H₃₂O₄P₂
badge Registry Numbers
MDL Number MFCD05861608
thermostat Physical Properties
Melting Point >260 °C
Boiling Point 738.4±60.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a tetrahydrobenzodioxin backbone and diphenylphosphino groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where it helps produce chiral compounds with high optical purity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure drugs, as well as in the production of fine chemicals and agrochemicals. The ligand's stability and ability to form robust complexes with metals like rhodium and ruthenium further enhance its utility in various catalytic processes.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,772.00
inventory 100mg
10-20 days ฿4,230.00

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R-()-6,6'-Bis(diphenylphosphino)-2,2',3,3'-tetrahydro-5,5'-bi-1,4-benzodioxin
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a tetrahydrobenzodioxin backbone and diphenylphosphino groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where it helps produce chiral compounds with high optical purity. Its application is significant in the pharmaceutical i

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a tetrahydrobenzodioxin backbone and diphenylphosphino groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, hydroformylation, and carbon-carbon bond-forming reactions, where it helps produce chiral compounds with high optical purity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure drugs, as well as in the production of fine chemicals and agrochemicals. The ligand's stability and ability to form robust complexes with metals like rhodium and ruthenium further enhance its utility in various catalytic processes.

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