![[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2-imidazolidinylidene]dichloro[[2-(1-methylethoxy)-5-[(2,2,…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFB104055.webp&w=3840&q=75)

[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2-imidazolidinylidene]dichloro[[2-(1-methylethoxy)-5-[(2,2,2-trifluoroacetyl)amino]phenyl]met hylene]-ruthenium
CAS:
Rif. 3D-FB104055
![[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2-imidazolidinylidene]dichloro[[2-(1-methylethoxy)-5-[(2,2,…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fproducts%2F3D%2Fthumb-webp%2FFB104055.webp&w=3840&q=75)

Informazioni sul prodotto
Nome:[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-2-imidazolidinylidene]dichloro[[2-(1-methylethoxy)-5-[(2,2,2-trifluoroacetyl)amino]phenyl]met hylene]-ruthenium
Marchio:Biosynth
Descrizione:Ruthenium-catalyzed metathesis reactions are used for the synthesis of organic molecules. This process is characterized by the formation of a metal-carbon bond, where the carbon atom moves from one organic molecule to another. The catalytic cycle starts with a proton transfer from an acid to the ruthenium catalyst, which then forms a covalent bond between the two reactants and releases an H+ ion. The newly formed intermediate is then attacked by another reactant molecule and undergoes a second proton transfer. The process is repeated until all of the reactants have been consumed.
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Proprietà chimiche
Peso molecolare:821.8 g/mol
Formula:C39H50Cl2F3N3O2Ru
Purezza:Min. 95%