Dichlorobis(2-(diisopropylphosphino)-ethylamine)ruthenium(II

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Reagent Code: #169657
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Alias Dichlorobis(2-(diisopropylphosphino)-ethylamine)ruthenium(II)
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CAS Number 1092372-90-1

science Other reagents with same CAS 1092372-90-1

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Weight 494.43 g/mol
Formula C₁₆H₄₀Cl₂N₂P₂Ru
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a highly efficient catalyst in hydrogenation reactions, particularly for the reduction of polar bonds such as carbonyl groups and imines. It shows excellent activity and selectivity in asymmetric synthesis, enabling the production of chiral amines and alcohols important in pharmaceutical intermediates. The complex is especially valued in transfer hydrogenation, where it facilitates the conversion of ketones and aldehydes to alcohols using hydrogen donors like formic acid or isopropanol. Its robust performance under mild reaction conditions makes it suitable for fine chemical and drug manufacturing processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,360.00
inventory 250mg
10-20 days ฿5,710.00
inventory 1g
10-20 days ฿16,670.00

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Dichlorobis(2-(diisopropylphosphino)-ethylamine)ruthenium(II
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Used as a highly efficient catalyst in hydrogenation reactions, particularly for the reduction of polar bonds such as carbonyl groups and imines. It shows excellent activity and selectivity in asymmetric synthesis, enabling the production of chiral amines and alcohols important in pharmaceutical intermediates. The complex is especially valued in transfer hydrogenation, where it facilitates the conversion of ketones and aldehydes to alcohols using hydrogen donors like formic acid or isopropanol. Its robus

Used as a highly efficient catalyst in hydrogenation reactions, particularly for the reduction of polar bonds such as carbonyl groups and imines. It shows excellent activity and selectivity in asymmetric synthesis, enabling the production of chiral amines and alcohols important in pharmaceutical intermediates. The complex is especially valued in transfer hydrogenation, where it facilitates the conversion of ketones and aldehydes to alcohols using hydrogen donors like formic acid or isopropanol. Its robust performance under mild reaction conditions makes it suitable for fine chemical and drug manufacturing processes.

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