(S)-2,2'-Bis-[(N,N’-diphenylphosphino)-amino]-1,1'-binaphthyl

≥98%,≥99% e.e.

Reagent Code: #65673
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CAS Number 74974-15-5

science Other reagents with same CAS 74974-15-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 652.7 g/mol
Formula C₄₄H₃₄N₂P₂
inventory_2 Storage & Handling
Storage room temperature, 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 enabling the synthesis of enantiomerically pure compounds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, where high enantioselectivity and yield are required. Additionally, it is employed in research and development to explore new catalytic processes and optimize existing ones for industrial applications.

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Size Availability Unit Price Quantity
inventory 2g
10-20 days ฿34,250.00
inventory 100mg
10-20 days ฿12,760.00

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(S)-2,2'-Bis-[(N,N’-diphenylphosphino)-amino]-1,1'-binaphthyl
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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 enabling the synthesis of enantiomerically pure compounds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, where high enantioselectivity and yield are required. Additionally, it is employed
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in enabling the synthesis of enantiomerically pure compounds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is prominent in hydrogenation, carbon-carbon bond formation, and other stereoselective transformations, where high enantioselectivity and yield are required. Additionally, it is employed in research and development to explore new catalytic processes and optimize existing ones for industrial applications.
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