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Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II)_Molecular_structure_CAS_635679-24-2)
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Dichloro[1,3-bis(2,6-isopropylphenyl)-2-imidazolidinylidene](2-isopropoxyphenylmethylene)ruthenium(II)

Catalog No. 729345 Name Sigma Aldrich
CAS Number 635679-24-2 Website http://www.sigmaaldrich.com
M. F. C37H50Cl2N2ORu Telephone 1-800-521-8956
M. W. 710.7817 Fax
Purity Email
Storage Chembase ID: 143342

SYNONYMS

IUPAC name
{1,3-bis[2,6-bis(propan-2-yl)phenyl]imidazolidin-2-ylidene}dichloro{[2-(propan-2-yloxy)phenyl]methylidene}ruthenium
IUPAC Traditional name
[1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene]dichloro[(2-isopropoxyphenyl)methylidene]ruthenium

DATABASE IDS

CAS Number 635679-24-2

PROPERTIES

Empirical Formula (Hill Notation) C37H50Cl2N2ORu
Melting Point 242-246 °C
MSDS Link Download
Storage Temperature 2-8°C
German water hazard class nwg

DETAILS

Description (English)
Packaging
100, 500 mg in glass bottle
2 g in glass bottle
Legal Information
US Patent No. 6,316,380 and 6,921,735 (and associated foreign equivalents of the foregoing) apply. Sale of this product conveys to the buyer a limited-use research license. For full details of this license please see sigma-aldrich.com/materialicense. For questions, please contact us at aldrich@sial.com or Materia at info@materia-inc.com.
Application

• Though slower to initiate than its phosphine analog 729353, it possesses similar reactivity.
• The preferred catalyst for making trisubstituted olefins by CM.1
Description (简体中文)
包装
100, 500 mg in glass bottle
2 g in glass bottle
Legal Information
US Patent No. 6,316,380 and 6,921,735 (and associated foreign equivalents of the foregoing) apply. Sale of this product conveys to the buyer a limited-use research license. For full details of this license please see sigma-aldrich.com/materialicense. For questions, please contact us at aldrich@sial.com or Materia at info@materia-inc.com.
Application

• Though slower to initiate than its phosphine analog 729353, it possesses similar reactivity.
• The preferred catalyst for making trisubstituted olefins by CM.1

REFERENCES