Pular para o conteúdo
Merck
Todas as fotos(4)

Documentos

682365

Sigma-Aldrich

Grubbs Catalyst® M207

Umicore

Sinônimo(s):

Dichloro[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene](3-methyl-2-butenylidene) (tricyclohexylphosphine)ruthenium(II), Grubbs Catalyst® M2b (C827), Isopentenylidene(1,3-dimesitylimidazolidin-2-ylidene) (tricyclohexylphosphine)ruthenium(II) dichloride, [SIMes]dichloro(3-methyl-2-butenylidene)(tricyclohexylphosphine)Ru(II)

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(4)

About This Item

Fórmula empírica (Notação de Hill):
C44H67Cl2N2PRu
Número CAS:
253688-91-4
Peso molecular:
826.97
Número MDL:
MFCD09265165
Código UNSPSC:
12161600
ID de substância PubChem:
24885711
NACRES:
NA.22

adequação da reação

core: ruthenium
reagent type: catalyst
reaction type: Olefin Metathesis

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

C1CCC(CC1)P(C2CCCCC2)C3CCCCC3.C\C(C)=C/C=[Ru](Cl)(Cl)=C4N(CCN4c5c(C)cc(C)cc5C)c6c(C)cc(C)cc6C

InChI

1S/C21H26N2.C18H33P.C5H8.2ClH.Ru/c1-14-9-16(3)20(17(4)10-14)22-7-8-23(13-22)21-18(5)11-15(2)12-19(21)6;1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-4-5(2)3;;;/h9-12H,7-8H2,1-6H3;16-18H,1-15H2;1,4H,2-3H3;2*1H;/q;;;;;+2/p-2

chave InChI

LCOFYVWULBZOTA-UHFFFAOYSA-L

Procurando produtos similares? Visita Guia de comparação de produtos

Descrição geral

Learn more about our metathesis catalysts

Aplicação

A general purpose olefin metathesis catalyst similar in reactivity to Grubbs Catalyst® 2nd Generation.

Outras notas

Grubbs Catalyst® Technology for Olefin Metathesis by Aldrich

Informações legais

Product of Umicore

Product License
This product, its manufacturing or use, is the subject of one or more issued or pending U.S. Patents (and foreign equivalents) owned or controlled by Umicore PMC. The purchase of this product from Umicore PMC through Sigma-Aldrich, its affiliates or their authorized distributors conveys to the buyer a limited, one-time, non-exclusive, non-transferable, non-assignable license. Buyer′s use of this product may infringe patents owned or controlled by third parties. It is the sole responsibility of buyer to ensure that its use of the product does not infringe the patent rights of third parties or exceed the scope of the license granted herein.

For any further information on product please refer to your local Umicore PMC contact at http://www.pmc.umicore.com
Grubbs Catalyst is a registered trademark of Umicore AG & Co. KG

Pictogramas

Flame
GHS02

Palavra indicadora

Warning

Frases de perigo

H228

Declarações de precaução

P210 - P240 - P241 - P280 - P370 + P378

Classificações de perigo

Flam. Sol. 2

Código de classe de armazenamento

4.1B - Flammable solid hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 2

1 of 2

Grubbs Catalyst® M101 Umicore

Sigma-Aldrich

774901

Grubbs Catalyst® M101

Hoveyda-Grubbs Catalyst® M2001 Umicore

Sigma-Aldrich

771082

Hoveyda-Grubbs Catalyst® M2001

Ryan P Murelli et al.
Organic letters, 9(9), 1749-1752 (2007-04-03)
[reaction: see text] In the presence of ruthenium-based olefin metathesis catalysts and triphenylphosphine, alpha,beta-unsaturated aldehydes can be olefinated with diazoacetates. This ruthenium-catalyzed transformation has been employed in tandem with olefin cross-metathesis to convert terminal olefins into 1,3-dienoic esters in a
Kevin M Kuhn et al.
Organic letters, 12(5), 984-987 (2010-02-10)
A series of ruthenium catalysts have been screened under ring-closing metathesis (RCM) conditions to produce five-, six-, and seven-membered carbamate-protected cyclic amines. Many of these catalysts demonstrated excellent RCM activity and yields with as low as 500 ppm catalyst loadings.
A K Chatterjee et al.
Organic letters, 1(11), 1751-1753 (2000-06-03)
[formula: see text] Trisubstituted alkenes have been prepared for the first time via intermolecular olefin cross-metathesis, using 1,3-dimesityl-4,5-dihydroimidazol-2-ylidene ruthenium alkylidene complexes 3a,b in good yields with moderate E selectivity. In addition, protected alcohols near the geminal disubstituted olefin improve reactivity
Schrodi, Y.; Pederson, R.L.
Aldrichimica Acta, 40, 45-45 (2007)
T M Trnka et al.
Accounts of chemical research, 34(1), 18-29 (2001-02-15)
In recent years, the olefin metathesis reaction has attracted widespread attention as a versatile carbon-carbon bond-forming method. Many new applications have become possible because of major advances in catalyst design. State-of-the-art ruthenium catalysts are not only highly active but also
Exibir todos os documentos relacionados

Conteúdo relacionado

Grubbs Group – Professor Product Portal

Research in the Grubbs group has centered on the development and application of a suite of highly active, selective, and bench stable ruthenium alkylidene complexes capable of catalyzing versatile olefin metatheses.

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica