(R)-(6,6'-Dimethoxy-[1,1'-biphenyl]-2,2'-diyl)bis(diphenylphosphine)

≥98%

Reagent Code: #68637
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CAS Number 133545-16-1

science Other reagents with same CAS 133545-16-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 582.61 g/mol
Formula C₃₈H₃₂O₂P₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and carbon-carbon bond formation reactions. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where achieving high enantiomeric purity is essential. Additionally, it is utilized in academic research to develop new catalytic methodologies and study stereochemical outcomes in organic synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,230.00
50mg
10-20 days ฿720.00
100mg
10-20 days ฿930.00
(R)-(6,6'-Dimethoxy-[1,1'-biphenyl]-2,2'-diyl)bis(diphenylphosphine)
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and carbon-carbon bond formation reactions. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where achieving high enantiomeric purity is essential. Additionally, it is utilized in academic research to develop new catalyti
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and carbon-carbon bond formation reactions. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where achieving high enantiomeric purity is essential. Additionally, it is utilized in academic research to develop new catalytic methodologies and study stereochemical outcomes in organic synthesis.
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