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Merck

196215

Sigma-Aldrich

Bis(cyclopentadienyl)zirconium(IV)-dichlorid

greener alternative

≥98%

Synonym(e):

Di-(cyclopentadienyl)-zirkonium-dichlorid, Zirkonocen-dichlorid

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About This Item

Empirische Formel (Hill-System):
C10H10Cl2Zr
CAS-Nummer:
Molekulargewicht:
292.32
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12161600
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

Assay

≥98%

Form

solid

Eignung der Reaktion

core: zirconium
reaction type: Polymerization Reactions
reagent type: catalyst
reaction type: Olefin Metathesis

Grünere Alternativprodukt-Eigenschaften

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Parameter

moisture sensitive

mp (Schmelzpunkt)

242-245 °C (lit.)

Grünere Alternativprodukt-Kategorie

Lagertemp.

2-8°C

SMILES String

Cl[Zr]Cl.[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2

InChI

1S/2C5H5.2ClH.Zr/c2*1-2-4-5-3-1;;;/h2*1-5H;2*1H;/q;;;;+2/p-2

InChIKey

QRUYYSPCOGSZGQ-UHFFFAOYSA-L

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Allgemeine Beschreibung

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Find details here.

Zirconocene dichloride serves as a catalyst, enabling efficient synthesis of pyrrole with high yields and simplifies the purification process economically.

Anwendung

Useful in the synthesis of a wide range of early-transition-metal complexes and organometallic compounds.
Used to promote greener amidations of carboxylic acids and amines in catalytic amounts. This technology avoids the requirement of preactivation of the carboxylic acid or use of coupling reagents.

Direct amide formation from unactivated carboxylic acids and amines

Piktogramme

Exclamation mark

Signalwort

Warning

Gefahreneinstufungen

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Sven Tobisch
Dalton transactions (Cambridge, England : 2003), (35)(35), 4277-4285 (2006-08-26)
The complete sequence of steps of a tentative catalytic cycle for intramolecular hydroamination/cyclisation (IHC) of 4,5-hexadien-1-ylamine (1) by a prototypical cationic [Cp(2)ZrCH(3)](+) zirconocene precatalyst (2) has been examined by employing a gradient-corrected DFT method. The predicted smooth overall reaction energy
Baekhap Choi et al.
Macromolecular rapid communications, 34(6), 533-538 (2013-01-29)
Catalytic natures of organometallic catalysts are modulated by coordinating organic ligands with proper steric and electronic properties to metal centers. Carbon-based nanomaterials such as graphene nanoplatelets are used with and without N-doping and multiwalled carbon nanotube as a ligand for
Andy M Chapman et al.
Journal of the American Chemical Society, 133(45), 18463-18478 (2011-10-01)
The extension of the frustrated Lewis pair (FLP) concept to the transition series with cationic zirconocene-phosphinoaryloxide complexes is demonstrated. Such complexes mimic the reactivity of main group FLPs in reactions such as heterolytic hydrogen cleavage, CO(2) activation, olefin and alkyne
José Barluenga et al.
Organic letters, 9(16), 3081-3084 (2007-07-20)
A new regio- and stereoselective zirconocene-catalyzed reaction for the synthesis of medium-sized rings is described. The global reaction supposes a formal ring expansion of a cyclic enol ether to give a functionalized carbocycle.
Peter Wipf et al.
Organic letters, 7(3), 483-485 (2005-01-28)
[reaction: see text] Hydrozirconation of terminal alkynes, followed by AgClO4-catalyzed in situ addition of the resultant alkenylzirconocenes to 1,2-anhydrosugars (glycal epoxides) leads to alpha-C-glycosides in moderate to high yields.

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