1,1'-[(5R)-2,2',3,3'-Tetrahydro[5,5'-bi-1,4-benzodioxin]-6,6'-diyl]bis[1,1-bis[3,5-bis(trifluoromethyl)phenyl]phosphine]

97%

Reagent Code: #229395
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CAS Number 1306747-75-0

science Other reagents with same CAS 1306747-75-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1182.63 g/mol
Formula C₄₈H₂₄F₂₄O₄P₂
thermostat Physical Properties
Melting Point 168 °C
Boiling Point 740.1±60.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its rigid, C2-symmetric structure enables high stereocontrol, making it valuable in the synthesis of chiral pharmaceuticals and fine chemicals. The electron-withdrawing trifluoromethyl groups enhance ligand stability and influence metal center reactivity. Commonly employed with rhodium or ruthenium complexes, it facilitates the production of single-enantiomer products in high yield and ee.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,110.00
inventory 250mg
10-20 days ฿22,290.00

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1,1'-[(5R)-2,2',3,3'-Tetrahydro[5,5'-bi-1,4-benzodioxin]-6,6'-diyl]bis[1,1-bis[3,5-bis(trifluoromethyl)phenyl]phosphine]
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its rigid, C2-symmetric structure enables high stereocontrol, making it valuable in the synthesis of chiral pharmaceuticals and fine chemicals. The electron-withdrawing trifluoromethyl groups enhance ligand stability and influence metal center reactivity. Commonly employed with rhodium or ruthenium complexes, it facilitates the production of single-enantiomer products in high yield and ee.

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its rigid, C2-symmetric structure enables high stereocontrol, making it valuable in the synthesis of chiral pharmaceuticals and fine chemicals. The electron-withdrawing trifluoromethyl groups enhance ligand stability and influence metal center reactivity. Commonly employed with rhodium or ruthenium complexes, it facilitates the production of single-enantiomer products in high yield and ee.

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