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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)

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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)
  • (SP-5-41)-[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2-imidazolidinylidene]dichloro[[2-(1-methylethoxy-κO)phenyl]methylene-κC]ruthenium
CAS:
635679-24-2
MF:
C37H49Cl2N2ORu
MW:
709.78
Mol File:
635679-24-2.mol
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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
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Safety Information

WGK Germany 
nwg
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Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II) Usage And Synthesis

Uses

Though slower to initiate than its phosphine analog 729353, it possesses similar reactivity. The preferred catalyst for making trisubstituted olefins by CM.

Uses

Preferred catalyst for making trisubstituted olefins by cross metathesis.

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

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