(S)-(-)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl

98.0%

Reagent Code: #68692
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CAS Number 134484-36-9

science Other reagents with same CAS 134484-36-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 468.54 g/mol
Formula C₃₃H₂₅OP
badge Registry Numbers
MDL Number MFCD00269686
thermostat Physical Properties
Melting Point 175-179°C
inventory_2 Storage & Handling
Storage room temperature

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 synthesis, enabling the production of optically active compounds with high selectivity. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations in organic synthesis. The compound is especially valuable in the pharmaceutical industry for creating chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is utilized in academic research to develop novel catalytic processes and study stereochemistry.

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Test Parameter Specification
Appearance White to off-white Solid
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,990.00
inventory 100mg
10-20 days ฿6,620.00

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(S)-(-)-2-Diphenylphosphino-2'-methoxy-1,1'-binaphthyl
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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 synthesis, enabling the production of optically active compounds with high selectivity. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other key transformations in organic synthesis. The compound is especially valuable in the pharmaceutical industry for creating chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it is utilized in academic research to develop novel catalytic processes and study stereochemistry.
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