Carbonylchlorohydrido[bis(2-di-cyclohexylphosphinoethyl)amine]ruthenium(II)

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Reagent Code: #61175
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CAS Number 1421060-11-8

science Other reagents with same CAS 1421060-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 631.22 g/mol
Formula C₂₉H₅₄ClNOP₂Ru
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This complex is primarily used in catalysis, particularly in hydrogenation and transfer hydrogenation reactions. It is effective in reducing various organic compounds, including ketones, aldehydes, and imines, to their corresponding alcohols or amines. Its stability and selectivity make it suitable for applications in fine chemical synthesis and pharmaceutical manufacturing. Additionally, it is employed in asymmetric catalysis to produce chiral molecules, which are crucial in the development of enantiomerically pure drugs. The compound’s robust structure allows it to operate under mild conditions, enhancing its utility in industrial processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,300.00

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Carbonylchlorohydrido[bis(2-di-cyclohexylphosphinoethyl)amine]ruthenium(II)
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This complex is primarily used in catalysis, particularly in hydrogenation and transfer hydrogenation reactions. It is effective in reducing various organic compounds, including ketones, aldehydes, and imines, to their corresponding alcohols or amines. Its stability and selectivity make it suitable for applications in fine chemical synthesis and pharmaceutical manufacturing. Additionally, it is employed in asymmetric catalysis to produce chiral molecules, which are crucial in the development of enantiome

This complex is primarily used in catalysis, particularly in hydrogenation and transfer hydrogenation reactions. It is effective in reducing various organic compounds, including ketones, aldehydes, and imines, to their corresponding alcohols or amines. Its stability and selectivity make it suitable for applications in fine chemical synthesis and pharmaceutical manufacturing. Additionally, it is employed in asymmetric catalysis to produce chiral molecules, which are crucial in the development of enantiomerically pure drugs. The compound’s robust structure allows it to operate under mild conditions, enhancing its utility in industrial processes.

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