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301224-40-8

301224-40-8 Structure

301224-40-8 Structure
IdentificationBack Directory
[Name]

(1,3-BIS-(2,4,6-TRIMETHYLPHENYL)-2-IMIDAZOLIDINYLIDENE)DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE)RUTHENIUM
[CAS]

301224-40-8
[Synonyms]

HOVEYDA-GRUBBS
Hoveyda-Grubbs 2nd
HOVEYDA-GRUBBS CATALYST
Hoveyda-Grubbs Catalyst 2nd
Hoveyda-Grubbs Catalyst 2nd Generation
301224-40-8
Hoveyda-Grubbs Catalyst 2nd Generation 97%
Hoveyda-Grubbs Catalyst 2nd Generation,97%
Dichloro(1,3-diMesityl-2-iMidazolidinylidene)(2-isopropoxybenzylidene)rutheniuM
(1,3-DiMesityliMidazolidin-2-ylidene)(2-isopropoxybenzylidene)rutheniuM(VI) chloride
[1,3-Bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(2-isopropoxyphenylmethylene)ruthenium
(1,3-Bis-(2,4,6-triMethylphenyl)-2-iMidazolidinylidene)dichloro (o-isopropylphenylMethylene)rutheniuM
(1,3-BIS-(2,4,6-TRIMETHYLPHENYL)-2-IMIDAZOLIDINYLIDENE)DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE)RUTHENIUM
(1,3-BIS-(2,4,6-TRIMETHYLPHENYL)-2-IMIDAZOLIDINYLIDENE)DICHLORO(O-ISOPROPOXYPHENYLMETHYLENE)RUTHENIUM
RUTHENIUM,[1,3-BIS(2,4,6-TRIMETHYLPHENYL)-2-IMIDAZOLIDINYLIDENE]DICHLORO[[2-(1-METHYLETHOXY)PHENYL]METHYLENE]
Hoveyda-Grubbs Catalyst 2nd Generation,(1,3-Bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene)dichloro(o-isopropoxyphenylmethylene)ruthenium
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C31H38Cl2N2ORu
[MDL Number]

MFCD03701614
[MOL File]

301224-40-8.mol
[Molecular Weight]

626.62
Chemical PropertiesBack Directory
[Melting point ]

216-220 °C(lit.)
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Dichloromethane (Slightly), Methanol (Slightly)
[form ]

Solid
[color ]

Green to Very Dark Green
[Stability:]

Hygroscopic
[InChIKey]

ZRPFJAPZDXQHSM-UHFFFAOYSA-L
[CAS DataBase Reference]

301224-40-8
[EPA Substance Registry System]

Ruthenium, [1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro[[2-(1-methylethoxy-.kappa.O)phenyl]methylene-.kappa.C]-, (SP-5-41)- (301224-40-8)
Hazard InformationBack Directory
[Chemical Properties]

Bright green crystalline powder
[Uses]

It′s a phosphine free version of Grubbs 2nd Generation Catalyst with comparable reactivity, but initiates more readily at lower temperatures. Efficient for metathesis of electron-deficient substrates including fluorinated olefins. Demonstrated in multiple large-scale pharmaceutical applications.
It can be used as a catalyst for olefin cross-metathesis with fluorinated olefins (CM), ring-closing metathesis (RCM), ring-opening metathesis (ROM), and a sequence of a metathesis reaction and subsequent dihydroxylation of the newly formed double bond.
Safety DataBack Directory
[WGK Germany ]

3
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