Dirhodium(II) tetrakis(caprolactam)

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Reagent Code: #170773
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CAS Number 138984-26-6

science Other reagents with same CAS 138984-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 654.41 g/mol
Formula C₂₄H₄₀N₄O₄Rh₂
badge Registry Numbers
MDL Number MFCD00467690
thermostat Physical Properties
Melting Point 196-200 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Widely used as a homogeneous catalyst in organic synthesis, particularly in cyclopropanation and C–H functionalization reactions. Its high selectivity and efficiency make it valuable in pharmaceutical manufacturing, where precise stereochemical control is critical. The caprolactam ligands enhance solubility in polar organic solvents, improving catalyst performance in reactions involving diazo compounds. It is also employed in the development of fine chemicals and asymmetric synthesis due to its ability to promote enantioselective transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,650.00
inventory 250mg
10-20 days ฿10,860.00

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Dirhodium(II) tetrakis(caprolactam)
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Widely used as a homogeneous catalyst in organic synthesis, particularly in cyclopropanation and C–H functionalization reactions. Its high selectivity and efficiency make it valuable in pharmaceutical manufacturing, where precise stereochemical control is critical. The caprolactam ligands enhance solubility in polar organic solvents, improving catalyst performance in reactions involving diazo compounds. It is also employed in the development of fine chemicals and asymmetric synthesis due to its ability t

Widely used as a homogeneous catalyst in organic synthesis, particularly in cyclopropanation and C–H functionalization reactions. Its high selectivity and efficiency make it valuable in pharmaceutical manufacturing, where precise stereochemical control is critical. The caprolactam ligands enhance solubility in polar organic solvents, improving catalyst performance in reactions involving diazo compounds. It is also employed in the development of fine chemicals and asymmetric synthesis due to its ability to promote enantioselective transformations.

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