ChemicalBook Product Catalog Organic Chemistry Heterocyclic Compounds Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II)

Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II)

Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) Basic information
Product Name:Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II)
Synonyms:Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II);Grubbs Catalyst C711;Grubbs Catalyst(TM) C711;Hoveyda-Grubbs Catalyst? M722;[1,3-Bis-(2,6-diisopropylphenyl)-2-imidazolidinylidene]dichloro(2-isopropoxybenzylidene)ruthenium(II)
CAS:635679-24-2
MF:C37H49Cl2N2ORu
MW:709.78
EINECS:
Product Categories:
Mol File:635679-24-2.mol
Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) Structure
Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) Chemical Properties
Melting point 242-246°C
storage temp. 2-8°C
Safety Information
WGK Germany nwg
MSDS Information
Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) Usage And Synthesis
UsesThough slower to initiate than its phosphine analog 729353, it possesses similar reactivity. The preferred catalyst for making trisubstituted olefins by CM.
UsesPreferred catalyst for making trisubstituted olefins by cross metathesis.
Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) Preparation Products And Raw materials
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