Tris(triphenylphosphine)ruthenium(II) dichloride

99.95% metals basis, ruthenium 10.2% minimum

Reagent Code: #240604
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Alias Tris(triphenylphosphine)ruthenium dichloride
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CAS Number 15529-49-4

science Other reagents with same CAS 15529-49-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 958.83 g/mol
Formula C₅₄H₄₅Cl₂P₃Ru
badge Registry Numbers
EC Number 239-569-7
MDL Number MFCD00013077
thermostat Physical Properties
Melting Point 159 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Tris(triphenylphosphine)ruthenium(II) dichloride is a versatile organometallic complex used as a catalyst in homogeneous catalysis. It is particularly employed in hydrogenation reactions, including the reduction of alkenes, alkynes, and dienes, as well as transfer hydrogenation of ketones and aldehydes under mild conditions. The compound also facilitates olefin isomerization and serves as a precursor for other ruthenium-based catalysts. Its phosphine ligands stabilize the ruthenium center, enhancing catalytic activity and selectivity. Widely applied in organic synthesis, pharmaceutical research, and fine chemicals production for efficient and selective transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,590.00
inventory 5g
10-20 days ฿13,780.00

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Tris(triphenylphosphine)ruthenium(II) dichloride
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Tris(triphenylphosphine)ruthenium(II) dichloride is a versatile organometallic complex used as a catalyst in homogeneous catalysis. It is particularly employed in hydrogenation reactions, including the reduction of alkenes, alkynes, and dienes, as well as transfer hydrogenation of ketones and aldehydes under mild conditions. The compound also facilitates olefin isomerization and serves as a precursor for other ruthenium-based catalysts. Its phosphine ligands stabilize the ruthenium center, enhancing cata

Tris(triphenylphosphine)ruthenium(II) dichloride is a versatile organometallic complex used as a catalyst in homogeneous catalysis. It is particularly employed in hydrogenation reactions, including the reduction of alkenes, alkynes, and dienes, as well as transfer hydrogenation of ketones and aldehydes under mild conditions. The compound also facilitates olefin isomerization and serves as a precursor for other ruthenium-based catalysts. Its phosphine ligands stabilize the ruthenium center, enhancing catalytic activity and selectivity. Widely applied in organic synthesis, pharmaceutical research, and fine chemicals production for efficient and selective transformations.

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