Tris(triphenylphosphine)rhodium(I) chloride

99.9% trace metals basis

Reagent Code: #239516
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CAS Number 14694-95-2

science Other reagents with same CAS 14694-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 925.22 g/mol
Formula C₅₄H₄₅ClP₃Rh
badge Registry Numbers
EC Number 238-744-5
MDL Number MFCD00010016
thermostat Physical Properties
Melting Point 245-250 °C(dec.)
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a homogeneous catalyst in various organic transformations, particularly in hydrogenation and hydroformylation reactions. It facilitates the addition of hydrogen across unsaturated bonds, such as alkenes and ketones, under mild conditions. Also employed in carbonylation and coupling reactions, where it promotes carbon-carbon bond formation. Its high selectivity and activity make it valuable in fine chemical synthesis and pharmaceutical manufacturing. Soluble in organic solvents, it enables efficient catalytic cycles in solution-phase systems. Often used in research and industrial processes requiring precise stereochemical control.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,980.00
inventory 1g
10-20 days ฿11,000.00
inventory 5g
10-20 days ฿30,000.00

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Tris(triphenylphosphine)rhodium(I) chloride
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Used as a homogeneous catalyst in various organic transformations, particularly in hydrogenation and hydroformylation reactions. It facilitates the addition of hydrogen across unsaturated bonds, such as alkenes and ketones, under mild conditions. Also employed in carbonylation and coupling reactions, where it promotes carbon-carbon bond formation. Its high selectivity and activity make it valuable in fine chemical synthesis and pharmaceutical manufacturing. Soluble in organic solvents, it enables efficie

Used as a homogeneous catalyst in various organic transformations, particularly in hydrogenation and hydroformylation reactions. It facilitates the addition of hydrogen across unsaturated bonds, such as alkenes and ketones, under mild conditions. Also employed in carbonylation and coupling reactions, where it promotes carbon-carbon bond formation. Its high selectivity and activity make it valuable in fine chemical synthesis and pharmaceutical manufacturing. Soluble in organic solvents, it enables efficient catalytic cycles in solution-phase systems. Often used in research and industrial processes requiring precise stereochemical control.

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