(S)-1-(Diphenylphosphino)-3-methylbutan-2-amine

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Reagent Code: #68663
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CAS Number 146476-37-1

science Other reagents with same CAS 146476-37-1

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scatter_plot Molecular Information
Weight 271.34 g/mol
Formula C₁₇H₂₂NP
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MDL Number MFCD17013993
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. Its ability to induce chirality in reactions makes it valuable for producing enantiomerically pure compounds, which are crucial in drug development. It is often employed in transition metal-catalyzed reactions, such as hydrogenation, where it enhances selectivity and efficiency. Additionally, it finds application in the preparation of complex organic molecules, contributing to advancements in medicinal chemistry and material science. Its stability and effectiveness in various catalytic systems make it a versatile tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,842.00
inventory 1g
10-20 days ฿29,520.00
inventory 250mg
10-20 days ฿9,720.00

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(S)-1-(Diphenylphosphino)-3-methylbutan-2-amine
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. Its ability to induce chirality in reactions makes it valuable for producing enantiomerically pure compounds, which are crucial in drug development. It is often employed in transition metal-catalyzed reactions, such as hydrogenation, where it enhances selectivity and efficiency. Additionally, it finds application in the preparation of complex organic molecules,

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in the synthesis of pharmaceuticals and fine chemicals. Its ability to induce chirality in reactions makes it valuable for producing enantiomerically pure compounds, which are crucial in drug development. It is often employed in transition metal-catalyzed reactions, such as hydrogenation, where it enhances selectivity and efficiency. Additionally, it finds application in the preparation of complex organic molecules, contributing to advancements in medicinal chemistry and material science. Its stability and effectiveness in various catalytic systems make it a versatile tool in organic synthesis.

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