(1R)-[1,1'-Binaphthalene]-2,2'-diylbis[bis[3,5-bis(1,1-dimethylethyl)phenyl]phosphine

98%

Reagent Code: #229064
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CAS Number 135139-01-4

science Other reagents with same CAS 135139-01-4

blur_circular Chemical Specifications

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Weight 1071.52 g/mol
Formula C₇₆H₉₆P₂
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation, cross-coupling, and C–H activation reactions. Its sterically bulky structure and well-defined chiral environment enhance selectivity and stability of metal catalysts, especially with rhodium, ruthenium, and palladium. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is required. The ligand’s rigidity and electron-rich phosphine groups facilitate efficient turnover and improved yield in asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿28,000.00

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(1R)-[1,1'-Binaphthalene]-2,2'-diylbis[bis[3,5-bis(1,1-dimethylethyl)phenyl]phosphine
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation, cross-coupling, and C–H activation reactions. Its sterically bulky structure and well-defined chiral environment enhance selectivity and stability of metal catalysts, especially with rhodium, ruthenium, and palladium. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is required. The ligand’s rigidity and electron-rich phosphine gro

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transformations such as hydrogenation, cross-coupling, and C–H activation reactions. Its sterically bulky structure and well-defined chiral environment enhance selectivity and stability of metal catalysts, especially with rhodium, ruthenium, and palladium. Commonly employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is required. The ligand’s rigidity and electron-rich phosphine groups facilitate efficient turnover and improved yield in asymmetric synthesis.

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