Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene][2-(1-methylacetoxy)phenyl]methyleneruthenium(II)

98%

Reagent Code: #174394
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CAS Number 1031262-71-1

science Other reagents with same CAS 1031262-71-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 654.638 g/mol
Formula C₃₂H₃₈Cl₂N₂O₂Ru
badge Registry Numbers
MDL Number MFCD22690885
thermostat Physical Properties
Melting Point 204-209 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as a highly efficient ruthenium-based metathesis catalyst, this compound enables ring-closing metathesis (RCM), cross metathesis (CM), and ring-opening metathesis polymerization (ROMP) in organic synthesis. It is particularly valued for its enhanced stability and activity in the formation of complex molecules, including pharmaceuticals, natural products, and advanced materials. The presence of the N-heterocyclic carbene (NHC) ligand improves catalyst longevity and functional group tolerance, allowing reactions to proceed under mild conditions with high yields. It is commonly employed in the synthesis of macrocyclic structures and olefin-rich frameworks where precision and reliability are critical. Its ease of handling and compatibility with various substrates make it a preferred choice in both academic research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,020.00
inventory 500mg
10-20 days ฿41,060.00

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Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene][2-(1-methylacetoxy)phenyl]methyleneruthenium(II)
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Widely used as a highly efficient ruthenium-based metathesis catalyst, this compound enables ring-closing metathesis (RCM), cross metathesis (CM), and ring-opening metathesis polymerization (ROMP) in organic synthesis. It is particularly valued for its enhanced stability and activity in the formation of complex molecules, including pharmaceuticals, natural products, and advanced materials. The presence of the N-heterocyclic carbene (NHC) ligand improves catalyst longevity and functional group tolerance,

Widely used as a highly efficient ruthenium-based metathesis catalyst, this compound enables ring-closing metathesis (RCM), cross metathesis (CM), and ring-opening metathesis polymerization (ROMP) in organic synthesis. It is particularly valued for its enhanced stability and activity in the formation of complex molecules, including pharmaceuticals, natural products, and advanced materials. The presence of the N-heterocyclic carbene (NHC) ligand improves catalyst longevity and functional group tolerance, allowing reactions to proceed under mild conditions with high yields. It is commonly employed in the synthesis of macrocyclic structures and olefin-rich frameworks where precision and reliability are critical. Its ease of handling and compatibility with various substrates make it a preferred choice in both academic research and industrial applications.

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