Chloro(p-cymene)[2-[(di-tert-butylphosphino)methyl]pyridine]ruthenium(II) Triflate

Carbon content: 43-48%

Reagent Code: #57926
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CAS Number 2058252-91-6

science Other reagents with same CAS 2058252-91-6

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scatter_plot Molecular Information
Weight 657.13 g/mol
Formula C₂₅H₃₈ClF₃NO₃PRuS
inventory_2 Storage & Handling
Storage room temperature, in an inert gas

description Product Description

This chemical is primarily used as a catalyst in various organic synthesis reactions, particularly in hydrogenation and transfer hydrogenation processes. It is highly effective in reducing ketones, aldehydes, and imines to their corresponding alcohols and amines, making it valuable in the production of pharmaceuticals and fine chemicals. Its robust structure and stability under reaction conditions allow for efficient and selective transformations. Additionally, it is employed in asymmetric synthesis, where it aids in creating chiral molecules, which are crucial in the development of active pharmaceutical ingredients (APIs). Its application extends to the synthesis of complex organic compounds, where it provides high yields and excellent enantioselectivity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,902.00

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Chloro(p-cymene)[2-[(di-tert-butylphosphino)methyl]pyridine]ruthenium(II) Triflate
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This chemical is primarily used as a catalyst in various organic synthesis reactions, particularly in hydrogenation and transfer hydrogenation processes. It is highly effective in reducing ketones, aldehydes, and imines to their corresponding alcohols and amines, making it valuable in the production of pharmaceuticals and fine chemicals. Its robust structure and stability under reaction conditions allow for efficient and selective transformations. Additionally, it is employed in asymmetric synthesis, whe

This chemical is primarily used as a catalyst in various organic synthesis reactions, particularly in hydrogenation and transfer hydrogenation processes. It is highly effective in reducing ketones, aldehydes, and imines to their corresponding alcohols and amines, making it valuable in the production of pharmaceuticals and fine chemicals. Its robust structure and stability under reaction conditions allow for efficient and selective transformations. Additionally, it is employed in asymmetric synthesis, where it aids in creating chiral molecules, which are crucial in the development of active pharmaceutical ingredients (APIs). Its application extends to the synthesis of complex organic compounds, where it provides high yields and excellent enantioselectivity.

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