(S)-1-(Diphenylphosphino)-3,3-dimethylbutan-2-amine

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Reagent Code: #68669
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CAS Number 286454-86-2

science Other reagents with same CAS 286454-86-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.36 g/mol
Formula C₁₈H₂₄NP
badge Registry Numbers
MDL Number MFCD17013995
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

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 the synthesis of enantiomerically pure compounds, which are important in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is prominent in hydrogenation reactions, where it helps achieve high enantioselectivity and yield. Additionally, it is utilized in cross-coupling reactions and other transformations that require precise control over stereochemistry. Its effectiveness in creating chiral centers makes it a valuable tool in the development of active pharmaceutical ingredients (APIs) and other complex organic molecules.

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Test Parameter Specification
APPEARANCE Colorless to Light yellow to Yellow Liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,032.00
inventory 250mg
10-20 days ฿8,352.00
inventory 1g
10-20 days ฿26,820.00

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(S)-1-(Diphenylphosphino)-3,3-dimethylbutan-2-amine
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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 the synthesis of enantiomerically pure compounds, which are important in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is prominent in hydrogenation reactions, where it helps achieve high enantioselectivity and yield. Additionally, it is utilized in cross-coupling reactions and other transformations that require p

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in the synthesis of enantiomerically pure compounds, which are important in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is prominent in hydrogenation reactions, where it helps achieve high enantioselectivity and yield. Additionally, it is utilized in cross-coupling reactions and other transformations that require precise control over stereochemistry. Its effectiveness in creating chiral centers makes it a valuable tool in the development of active pharmaceutical ingredients (APIs) and other complex organic molecules.

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