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)
- (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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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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