(S)-1-Amino-8-(diphenylphosphino)-1,2,3,4-tetrahydronaphthalene

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Reagent Code: #38597
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CAS Number 1222630-45-6

science Other reagents with same CAS 1222630-45-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 331.3906 g/mol
Formula C₂₂H₂₂NP
badge Registry Numbers
MDL Number MFCD17013991
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring a diphenylphosphino group and a chiral tetrahydronaphthalene backbone, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, hydroformylation, and cross-coupling reactions, where it helps produce chiral molecules with high optical purity. Its application is significant in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where enantiomeric purity is critical. Additionally, it is used in academic and industrial research to explore new catalytic processes and optimize existing ones.

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inventory 50mg
10-20 days ฿2,061.00

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(S)-1-Amino-8-(diphenylphosphino)-1,2,3,4-tetrahydronaphthalene
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring a diphenylphosphino group and a chiral tetrahydronaphthalene backbone, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, hydroformylation, and cross-coupling reactions, where it helps produce chiral molecules with high optical purity. Its application is significant in the synthesis of pharmaceutical

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its structure, featuring a diphenylphosphino group and a chiral tetrahydronaphthalene backbone, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, hydroformylation, and cross-coupling reactions, where it helps produce chiral molecules with high optical purity. Its application is significant in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where enantiomeric purity is critical. Additionally, it is used in academic and industrial research to explore new catalytic processes and optimize existing ones.

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