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Sigma-Aldrich

Hoveyda-Grubbs Catalyst® M721 ChemBeads

Sinonimo/i:

Hoveyda-Grubbs Catalyst®M72 SI(o-Tol) (C571)

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About This Item

Formula empirica (notazione di Hill):
C27H30Cl2N2ORu
Numero CAS:
Peso molecolare:
570.52
Numero MDL:
Codice UNSPSC:
12352100

Stato

solid

Livello qualitativo

Composizione

, 4-6 wt. % (loading of catalyst)

Impiego in reazioni chimiche

reagent type: catalyst
core: ruthenium
reaction type: Ring-Opening Polymerization

Stringa SMILE

Cl[Ru](C1N(C2=CC=CC=C2C)CCN1C3=CC=CC=C3C)(O4C(C)C)(Cl)=CC5=C4C=CC=C5

InChI

1S/C17H19N2.C10H12O.2ClH.Ru/c1-14-7-3-5-9-16(14)18-11-12-19(13-18)17-10-6-4-8-15(17)2;1-8(2)11-10-7-5-4-6-9(10)3;;;/h3-10,13H,11-12H2,1-2H3;3-8H,1-2H3;2*1H;/q;;;;+2/p-2
AFQRYTARHOMPFY-UHFFFAOYSA-L

Descrizione generale

Less sterically hindered analog of Hoveyda-Grubbs Catalyst® 2nd Generation. Excels at ring-closing metathesis reactions of sterically encumbered olefins. Also useful for the cross metathesis of olefins bearing large allylic substituents. ChemBeads are chemical coated glass beads. ChemBeads offer improved flowability and chemical uniformity perfect for automated solid dispensing and high-throughput experimentation. The method of creating ChemBeads uses no other chemicals or surfactants allowing the user to accurately dispense sub-milligram amounts of chemical.

Note legali

Grubbs Catalyst is a registered trademark of Umicore AG & Co. KG

Prodotti correlati

Codice della classe di stoccaggio

13 - Non Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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David E White et al.
Journal of the American Chemical Society, 130(3), 810-811 (2008-01-01)
Described in this report is the first total synthesis of elatol, a halogenated sesquiterpene in the chamigrene natural product family. The key disconnections in our synthetic approach include an enantioselective decarboxylative allylation to form the all-carbon quaternary stereocenter and a
Ian C Stewart et al.
Organic letters, 9(8), 1589-1592 (2007-03-24)
[reaction: see text] A series of ruthenium-based metathesis catalysts with N-heterocyclic carbene (NHC) ligands have been prepared in which the N-aryl groups have been changed from mesityl to mono-ortho-substituted phenyl (e.g., tolyl). These new catalysts offer an exceptional increase in

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