Determine the necessary mass, volume, or concentration for preparing a solution.
≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Product class
M-P, Homogeneous Catalysts, Grubbs Catalyst® 1st Generation, Phosphorus Ligands - Achiral
Reaction type
Alkene Metathesis, Cross Metathesis, Enyne Metathesis, Ring Closing Metathesis, Ring Opening Metathesis Polymerization, Self Metathesis
Chemical properties
C39H56Cl2P2Ru
Ru(iBu-phobane)2(Ind)Cl2
758.79
Ru
13
powder
brown
Applications & references
Total synthesis of macrocyclic HCV protease inhibitor with RCM as key step.
Reference: US2009 0163706
Ring opening metathesis polymerization.
Reference: Adv. Synth. Catal. 2010, 352, 1934 (DOI: 10.1002/adsc.201000207)
Ring closing metathesis forming heterocycles.
Reference: J. Org. Chem. 2008, 73, 259 (DOI: 10.1021/jo702169p)
Enyne cycloisomerization.
Reference: J. Org. Chem. 2008, 73, 259 (DOI: 10.1021/jo702169p)
Ethenolysis of methyl oleate.
Reference: Chem. Comm. 2008, 2726 (DOI: 10.1039/B718287B)
Self metathesis of terminal alkenes.
Reference: J. Org. Chem. 2008, 73, 259 (DOI: 10.1021/jo702169p)
| Canonical Smiles | CC(C)CP1C2CCCC1CCC2.CC(C)CP1C2CCCC1CCC2.C1=CC=C(C=C1)C2=CC(=[Ru](Cl)Cl)C3=CC=CC=C32 |
|---|---|
| IUPAC Name | dichloro-(3-phenylinden-1-ylidene)ruthenium;9-(2-methylpropyl)-9-phosphabicyclo[3.3.1]nonane |
| InChIKey | CCCYSKLUNSOBHP-UHFFFAOYSA-L |
| INCHI | 1S/C15H10.2C12H23P.2ClH.Ru/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)15;2*1-10(2)9-13-11-5-3-6-12(13)8-4-7-11;;;/h1-9,11H;2*10-12H,3-9H2,1-2H3;2*1H;/q;;;;;+2/p-2 |
| WGK Germany | 3 |
| PubChem CID | 124202843 |
| Molecular Weight | 758.78 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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