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

98%

Reagent Code: #57566
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CAS Number 70223-77-7

science Other reagents with same CAS 70223-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 480.559882 g/mol
Formula C₃₂H₃₄P₂
badge Registry Numbers
MDL Number MFCD00040557
thermostat Physical Properties
Boiling Point 588.1±23.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, where it helps produce chiral molecules with high selectivity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure compounds, which are essential for active pharmaceutical ingredients (APIs). Additionally, it is employed in organic chemistry research to develop new catalytic processes and optimize existing ones for improved efficiency and selectivity.

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Test Parameter Specification
Appearance colorless oil or white solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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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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(1S,2S)-()-1,2-BIS(DIPHENYLPHOSPHINOMETHYL)CYCLOHEXANE
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This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, where it helps produce chiral molecules with high selectivity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure compounds, which are essential for active pharmaceutical ingredients (APIs). Additionally, it is employed in organic chemistry research

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, where it helps produce chiral molecules with high selectivity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure compounds, which are essential for active pharmaceutical ingredients (APIs). Additionally, it is employed in organic chemistry research to develop new catalytic processes and optimize existing ones for improved efficiency and selectivity.

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