(1R,2R)-(-)-1,2-BIS(DIPHENYLPHOSPHINOMETHYL)CYCLOHEXANE

98%

Reagent Code: #57590
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CAS Number 70774-28-6

science Other reagents with same CAS 70774-28-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 480.56 g/mol
Formula C₃₂H₃₄P₂
badge Registry Numbers
MDL Number MFCD01073890
thermostat Physical Properties
Boiling Point 588.1±23.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high selectivity, which are essential in pharmaceuticals and fine chemicals. Its application extends to carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation and hydroformylation, where it ensures the formation of products with specific stereochemistry. Additionally, it is employed in the synthesis of complex organic compounds, contributing to the development of advanced materials and bioactive molecules.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White Solid
Purity (%) 97.5-100
Specific Rotation[A]20/D (C=1.07 Toluene)(°) -53.5--47.5
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿6,372.00
inventory 50mg
10-20 days ฿25,200.00

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(1R,2R)-(-)-1,2-BIS(DIPHENYLPHOSPHINOMETHYL)CYCLOHEXANE
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high selectivity, which are essential in pharmaceuticals and fine chemicals. Its application extends to carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation and hydroformylation, where it ensures the formation of products with specific stereochemistry. Ad

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enantioselective hydrogenation, where it helps produce chiral molecules with high selectivity, which are essential in pharmaceuticals and fine chemicals. Its application extends to carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation and hydroformylation, where it ensures the formation of products with specific stereochemistry. Additionally, it is employed in the synthesis of complex organic compounds, contributing to the development of advanced materials and bioactive molecules.

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