(2R,2'R,3R,3'R)-3,3'-di-tert-butyl-4,4'-bis((R)-2-methyl-1-phenylpropoxy)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole

97%, 99%ee

Reagent Code: #229168
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CAS Number 2376521-83-2

science Other reagents with same CAS 2376521-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 682.33 g/mol
Formula C₄₂H₅₂O₄P₂
badge Registry Numbers
MDL Number MFCD34597795
thermostat Physical Properties
Boiling Point 744.1±60.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, well-defined stereochemistry enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in rhodium- and ruthenium-based catalytic systems, it helps achieve high ee (enantiomeric excess) in the production of chiral intermediates. Also employed in academic research to develop new asymmetric transformations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿17,590.00
inventory 100mg
10-20 days ฿43,990.00

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(2R,2'R,3R,3'R)-3,3'-di-tert-butyl-4,4'-bis((R)-2-methyl-1-phenylpropoxy)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, well-defined stereochemistry enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in rhodium- and ruthenium-based catalytic systems, it helps achieve high ee (enantiomeric excess) in the production of chiral intermediates. Also employed in academic research to deve

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, well-defined stereochemistry enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in rhodium- and ruthenium-based catalytic systems, it helps achieve high ee (enantiomeric excess) in the production of chiral intermediates. Also employed in academic research to develop new asymmetric transformations.

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