Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II)

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Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II) Basic information
Product Name:Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II)
Synonyms:RUTHENIUM, DICHLORO[[2-(1-METHYLETHOXY)PHENYL]METHYLENE](TRICYCLOHEXYLPHOSPHINE);Dichloro[[2-(1-methylethoxy-O)phenyl]methylene](tricyclohexylphosphine)ruthenium;DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE) &;Dichloro(2-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium (II);Hoveyda-Grubbs Catalyst 1st Generation,Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II);RutheniuM,dichloro[[2-(1-Methylethoxy-kO)phenyl]Methylene-kC](tricyclohexylphosphine)-,(SP-5-41)-;Dichloro(2-isopropoxyphenylMethylene)(tricyclohexylphosphine)rutheniuM (II) (Hoveyda-Grubbs Catalyst 1st Generation);Hoveyda-Grubbs Catalyst 1st Generation
CAS:203714-71-0
MF:C28H45Cl2OPRu
MW:600.61
EINECS:692-988-0
Product Categories:Ru
Mol File:203714-71-0.mol
Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II) Structure
Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II) Chemical Properties
Melting point 195-197 °C(lit.)
storage temp. 2-8°C
solubility Chloroform (Slightly), Ethyl Acetate (Slightly)
form Solid
color Very Dark Purple
InChI1S/C18H33P.C10H12O.2ClH.Ru/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-8(2)11-10-7-5-4-6-9(10)3;;;/h16-18H,1-15H2;3-8H,1-2H3;2*1H;/q;;;;+2/p-2
InChIKeyKMKCJXPECJFQPQ-UHFFFAOYSA-L
SMILESP(C1CCCCC1)(C1CCCCC1)C1CCCCC1.C1(C=[Ru](Cl)Cl)=CC=CC=C1OC(C)C
Safety Information
Hazard Codes F
Risk Statements 11
RIDADR UN1325 - class 4.1 - PG 2 - Flammable solids, organic, n.o.s., HI: all
WGK Germany 3
Storage Class4.1B - Flammable solid hazardous materials
Hazard ClassificationsFlam. Sol. 2
MSDS Information
ProviderLanguage
SigmaAldrich English
Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II) Usage And Synthesis
UsesProven to be useful in Ring-Closing Metathesis (RCM) to form macrocycles. Also employed in a pivotal, macrocyclic ring-closing metathesis in the multi-step synthesis of an HCV protease inhibitor.
reaction suitabilitycore: ruthenium
reagent type: catalyst
reaction type: Ring Opening Metathesis Polymerisation
Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II) Preparation Products And Raw materials
Raw materialsBenzylidene-bis(tricyclohexylphosphine)dichlororuthenium-->Benzene, 1-ethenyl-2-(1-Methylethoxy)-
Tag:Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II)(203714-71-0) Related Product Information
(1,3-Bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(o-isopropoxyphenylmethylene)ruthenium Bis(triphenylphosphine)palladium(II) chloride Tetrakis(triphenylphosphine)palladium Bis(di-tert-butyl(4-dimethylaminophenyl)phosphine)dichloropalladium(II) [1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) 1,1'-Bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex 1,1'-Bis (di-t-butylphosphino)ferrocene palladium dichloride, Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene](benzylidene)bis(3-bromopyridine)ruthenium(II) Grubbs catalyst 2nd generation Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II) ruthenium, dichloro-[[2-isopropoxy-5-(n-dimethylamino-sulfonyl)phenyl]methylene](tricyclohexylphosphine) Tricyclohexyl phosphine