(p-Cymene)bis(mesitylcarboxylato)ruthenium(II)

Carbon content: 61-67%

Reagent Code: #161375
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CAS Number 1251667-99-8

science Other reagents with same CAS 1251667-99-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 561.6799999999999 g/mol
Formula C₃₀H₃₆O₄Ru
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a catalyst in olefin metathesis reactions, particularly effective in ring-closing metathesis (RCM) and cross-metathesis (CM) transformations. Exhibits high activity and stability under ambient conditions, making it suitable for synthesizing cyclic olefins and complex organic molecules in pharmaceutical and polymer chemistry. Tolerates a variety of functional groups, allowing its use in late-stage transformations of sensitive substrates. Often employed in academic and industrial research for developing new synthetic routes due to its ease of handling and reliable performance.

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Test Parameter Specification
Appearance Light yellow to yellow to orange to brown powder to crystal
Elemental Analysis (Carbon) 61-67
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,970.00

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(p-Cymene)bis(mesitylcarboxylato)ruthenium(II)
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Used as a catalyst in olefin metathesis reactions, particularly effective in ring-closing metathesis (RCM) and cross-metathesis (CM) transformations. Exhibits high activity and stability under ambient conditions, making it suitable for synthesizing cyclic olefins and complex organic molecules in pharmaceutical and polymer chemistry. Tolerates a variety of functional groups, allowing its use in late-stage transformations of sensitive substrates. Often employed in academic and industrial research for devel

Used as a catalyst in olefin metathesis reactions, particularly effective in ring-closing metathesis (RCM) and cross-metathesis (CM) transformations. Exhibits high activity and stability under ambient conditions, making it suitable for synthesizing cyclic olefins and complex organic molecules in pharmaceutical and polymer chemistry. Tolerates a variety of functional groups, allowing its use in late-stage transformations of sensitive substrates. Often employed in academic and industrial research for developing new synthetic routes due to its ease of handling and reliable performance.

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