| Identification | Back Directory | [Name]
DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE)(TRICYCLOHEXYLPHOSPHINE)RUTHENIUM(II) | [CAS]
203714-71-0 | [Synonyms]
Hoveyda-Grubbs G1
Hoveyda-Grubbs 1st
HOVEYDA-GRUBBS CATALYST 1ST
HOVEYDA-GRUBBS CATALYST 1ST GENERATION
Hoveyda-Grubbs Catalyst 2st Generation
DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE) &
Hoveyda-Grubbs Catalyst(TM) 1st Generation
Hoveyda-Grubbs Catalyst 1st Generation
Dichloro(2-isopropoxyphenylmethylene)(tricyclohexylp
dichloro{[2-(1-methylethoxy)phenyl]methylidene}ruthenium - t...
Dichloro(2-isopropoxybenzylidene)(tricyclohexylphosphine)ruthenium(II)
DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE)(TRICYCLOHEXYLPHOSPHINE)RUTHENIUM(II)
Dichloro(2-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium (II)
dichloro-[(2-propan-2-yloxyphenyl)methylidene]ruthenium,tricyclohexylphosphane
RUTHENIUM, DICHLORO[[2-(1-METHYLETHOXY)PHENYL]METHYLENE](TRICYCLOHEXYLPHOSPHINE)
Dichloro[[2-(1-methylethoxy-O)phenyl]methylene](tricyclohexylphosphine)ruthenium
dichloro{[2-(1-methylethoxy)phenyl]methylidene}ruthenium - tricyclohexylphosphane (1:1)
RutheniuM,dichloro[[2-(1-Methylethoxy-kO)phenyl]Methylene-kC](tricyclohexylphosphine)-,(SP-5-41)-
Hoveyda-Grubbs Catalyst 1st Generation,Dichloro(o-isopropoxyphenylmethylene)(tricyclohexylphosphine)ruthenium(II)
Dichloro(2-isopropoxyphenylMethylene)(tricyclohexylphosphine)rutheniuM (II) (Hoveyda-Grubbs Catalyst 1st Generation) | [EINECS(EC#)]
692-988-0 | [Molecular Formula]
C28H45Cl2OPRu | [MDL Number]
MFCD03453042 | [MOL File]
203714-71-0.mol | [Molecular Weight]
600.61 |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS02 | [Signal word ]
Warning | [Hazard statements ]
H228 | [Precautionary statements ]
P210 | [Hazard Codes ]
F | [Risk Statements ]
11 | [RIDADR ]
UN1325 - class 4.1 - PG 2 - Flammable solids, organic, n.o.s., HI: all | [WGK Germany ]
3 |
| Hazard Information | Back Directory | [Uses]
Proven 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. |
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