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3-Phenyl-1H-inden-1-ylidene[bis(i-butylphobane)]ruthenium(II) dichloride - 95%, high purity , CAS No.894423-99-5

COA

Grade & Purity:

≥95%

Cas Number: 894423-99-5
Molecular Weight: 758.78
MDL number: MFCD09264277
PubChem CID: 124202843

In stock

Item Number

P282788

Grouped product items
SKU	Size	Availability	Price	Qty
P282788-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$68.90
P282788-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$205.90

Discover 3-Phenyl-1H-inden-1-ylidene[bis(i-butylphobane)]ruthenium(II) dichloride by Aladdin Scientific in 95% for only $68.90. Available - in Ligands at Aladdin Scientific. Catalysts & Chiral Catalysts Tags: .

Basic Description

Synonyms	Umicore Grubbs Catalyst M110 \| Dichloro(3-phenyl-1H-inden-1-ylidene)bis(isobutylphobane)ruthenium(II), Dichlorobis(9-isobutyl-9-phosphabicyclo[3.3.1]nonane)(3-phenyl-1H-inden-1-ylidene)ruthenium(II), Grubbs Catalyst® M11
Specifications & Purity	≥95%
Legal Information	Sold in collaboration with Umicore for research purposes only. Patent US 10,518,716.
Product Description	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 Chemical formula C39H56Cl2P2Ru Empirical formula Ru(iBu-phobane)2(Ind)Cl2 Molecular weight 758.79 Metal Ru Theoretical metal content 13 Physical state powder Color 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)

Names and Identifiers

IUPAC Name	dichloro-(3-phenylinden-1-ylidene)ruthenium;9-(2-methylpropyl)-9-phosphabicyclo[3.3.1]nonane
INCHI	InChI=1S/C15H10.2C12H23P.2ClH.Ru/c1-2-6-12(7-3-1)15-11-10-13-8-4-5-9-14(13)15;21-10(2)9-13-11-5-3-6-12(13)8-4-7-11;;;/h1-9,11H;210-12H,3-9H2,1-2H3;2*1H;/q;;;;;+2/p-2
InChIKey	CCCYSKLUNSOBHP-UHFFFAOYSA-L
Smiles	CC(C)CP1C2CCCC1CCC2.CC(C)CP1C2CCCC1CCC2.C1=CC=C(C=C1)C2=CC(=[Ru](Cl)Cl)C3=CC=CC=C32
WGK Germany	3
PubChem CID	124202843
Molecular Weight	758.78

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