(1R,2R)-1-(Diphenylphosphino)-1-phenylpropan-2-amine

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Reagent Code: #68601
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CAS Number 799297-44-2

science Other reagents with same CAS 799297-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.38 g/mol
Formula C₂₁H₂₂NP
badge Registry Numbers
MDL Number MFCD17018768
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 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 significant in the pharmaceutical industry for the synthesis of chiral drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it is employed in the development of fine chemicals and agrochemicals, where precise control over stereochemistry is essential. Its robust performance in various catalytic processes, including hydrogenation and cross-coupling reactions, makes it a valuable tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,312.00
inventory 250mg
10-20 days ฿6,660.00
inventory 1g
10-20 days ฿23,643.00

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(1R,2R)-1-(Diphenylphosphino)-1-phenylpropan-2-amine
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This chemical is primarily 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 significant in the pharmaceutical industry for the synthesis of chiral drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it is employed in the development

This chemical is primarily 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 significant in the pharmaceutical industry for the synthesis of chiral drugs, where the specific spatial arrangement of atoms can greatly influence the drug's efficacy and safety. Additionally, it is employed in the development of fine chemicals and agrochemicals, where precise control over stereochemistry is essential. Its robust performance in various catalytic processes, including hydrogenation and cross-coupling reactions, makes it a valuable tool in organic synthesis.

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