(S)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amine

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Reagent Code: #70459
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CAS Number 259260-33-8

science Other reagents with same CAS 259260-33-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 453.513421 g/mol
Formula C₃₂H₂₄NP
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(S)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amine is widely used in asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure pharmaceuticals and fine chemicals. Its application is prominent in hydrogenation, cross-coupling, and C-H activation reactions, where it enhances selectivity and efficiency. The compound is also utilized in the development of advanced materials and organic semiconductors due to its unique electronic properties. Its role in academic and industrial research is significant for exploring new catalytic processes and optimizing existing ones.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿6,012.00
inventory 50mg
10-20 days ฿23,868.00

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(S)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amine
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(S)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amine is widely used in asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure pharmaceuticals and fine chemicals. Its application is prominent in hydrogenation, cross-coupling, and C-H activation reactions, where it enhances selectivity and efficiency. The compound is also utilized in the development of advanced materials a

(S)-2'-(Diphenylphosphino)-[1,1'-binaphthalen]-2-amine is widely used in asymmetric catalysis, particularly in the synthesis of chiral compounds. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure pharmaceuticals and fine chemicals. Its application is prominent in hydrogenation, cross-coupling, and C-H activation reactions, where it enhances selectivity and efficiency. The compound is also utilized in the development of advanced materials and organic semiconductors due to its unique electronic properties. Its role in academic and industrial research is significant for exploring new catalytic processes and optimizing existing ones.

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