(S)-(-)-2,2'-Bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl

98%

Reagent Code: #235879
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CAS Number 139139-93-8

science Other reagents with same CAS 139139-93-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 630.74 g/mol
Formula C₄₄H₄₀P₂
badge Registry Numbers
MDL Number MFCD01630795
thermostat Physical Properties
Melting Point 207-208 °C
Boiling Point 745.626 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation, carbon-carbon bond formation, and hydrosilylation reactions. Its rigid, sterically defined structure enhances stereocontrol, making it especially effective in producing single-enantiomer products in pharmaceutical synthesis and fine chemicals. Commonly employed with transition metals like rhodium, ruthenium, and palladium, it enables high catalytic activity and excellent enantioselectivity under mild conditions. Its applications extend to industrial-scale processes where optical purity is critical.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,300.00
inventory 250mg
10-20 days ฿7,370.00

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(S)-(-)-2,2'-Bis(diphenylphosphino)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation, carbon-carbon bond formation, and hydrosilylation reactions. Its rigid, sterically defined structure enhances stereocontrol, making it especially effective in producing single-enantiomer products in pharmaceutical synthesis and fine chemicals. Commonly employed with transition metals like rhodium, ruthenium, and palladium, it enables high catalytic activity and

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation, carbon-carbon bond formation, and hydrosilylation reactions. Its rigid, sterically defined structure enhances stereocontrol, making it especially effective in producing single-enantiomer products in pharmaceutical synthesis and fine chemicals. Commonly employed with transition metals like rhodium, ruthenium, and palladium, it enables high catalytic activity and excellent enantioselectivity under mild conditions. Its applications extend to industrial-scale processes where optical purity is critical.

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