(S)-6,6'-Bis(diphenylphosphino)-2,2',3,3'-tetrahydro-5,5'-bibenzo[b][1,4]dioxine

98%

Reagent Code: #68678
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CAS Number 503538-68-9

science Other reagents with same CAS 503538-68-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 638.63 g/mol
Formula C₄₀H₃₂O₄P₂
badge Registry Numbers
MDL Number MFCD05861608
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to effectively induce chirality in the synthesis of complex organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The ligand's ability to form stable complexes with metals like rhodium, iridium, and palladium enhances catalytic efficiency and selectivity, enabling the synthesis of enantiomerically pure compounds. This is especially crucial in the development of active pharmaceutical ingredients (APIs) where specific enantiomers often exhibit desired biological activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,745.00
inventory 250mg
10-20 days ฿8,802.00

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(S)-6,6'-Bis(diphenylphosphino)-2,2',3,3'-tetrahydro-5,5'-bibenzo[b][1,4]dioxine
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to effectively induce chirality in the synthesis of complex organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The ligand's ability to form stable complexes with metals like rhodium

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure allows it to effectively induce chirality in the synthesis of complex organic molecules, making it valuable in the production of pharmaceuticals and fine chemicals. It is often employed in asymmetric hydrogenation, carbon-carbon bond formation, and other stereoselective transformations. The ligand's ability to form stable complexes with metals like rhodium, iridium, and palladium enhances catalytic efficiency and selectivity, enabling the synthesis of enantiomerically pure compounds. This is especially crucial in the development of active pharmaceutical ingredients (APIs) where specific enantiomers often exhibit desired biological activity.

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