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Key Documents

Otros documentos

196215

Sigma-Aldrich

Bis(cyclopentadienyl)zirconium(IV) dichloride

greener alternative

≥98%

Sinónimos:

Dichlorodicyclopentadienylzirconium, Dichlorozirconocene, Zirconium dicyclopentadiene dichloride, Di(cyclopentadienyl)zirconium(IV) dichloride, Zirconocene dichloride

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About This Item

Fórmula empírica (notación de Hill):
C10H10Cl2Zr
Número de CAS:
1291-32-3
Peso molecular:
292.32
EC Number:
215-066-8
MDL number:
MFCD00003726
UNSPSC Code:
12352300
PubChem Substance ID:
24851743
NACRES:
NA.22

Quality Level

100

assay

≥98%

form

solid

reaction suitability

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

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

mp

242-245 °C (lit.)

greener alternative category

, Aligned

storage temp.

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

InChI key

QRUYYSPCOGSZGQ-UHFFFAOYSA-L

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Categorías relacionadas

General description

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.

Application

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
Useful in the synthesis of a wide range of early-transition-metal complexes and organometallic compounds.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificados de análisis (COA)

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Yuushou Nakayama et al.
Molecules (Basel, Switzerland), 10(6), 620-633 (2007-11-17)
This review article describes developments in chiral metallocenes as polymerization catalysts focusing on C2 symmetric ansa-zirconocene complexes. Selective synthesis of rac-isomers of ansa-zirconocenes are surveyed. Isospecific polymerizations of propylene catalyzed by chiral zirconocenes are summarized. Advanced series of polymerizations by
Shaoguang Zhang et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(46), 12608-12617 (2009-11-03)
A zirconocene-mediated one-pot multicomponent synthesis process leading to the synthesis of pyrrolo[3,2-c]pyridine (5-azaindoles) and pyrrole derivatives has been developed starting from a silicon-tethered diyne and three or two different or identical organonitriles. Pyrrolo[3,2-c]pyridine and pyrrole derivatives with diverse structures and
Anita Lagutschenkov et al.
The journal of physical chemistry. A, 114(5), 2073-2079 (2010-01-21)
Cationic zirconocene complexes are active species in Ziegler-Natta catalysis for olefin polymerization. Their structure and metal-ligand bond strength strongly influence their activity. In the present work, the infrared multiphoton dissociation (IRMPD) spectrum of mass selected Zr(C(5)H(5))(2)(OH)(CH(3)CN)(+) cations was obtained in
Aldrichimica Acta, 17, 28-28 (1984)
Benjamin N Atkinson et al.
Chemical communications (Cambridge, England), 48(95), 11626-11628 (2012-10-26)
Zirconocene dichloride (Cp(2)ZrCl(2)) has been shown to be an effective catalyst for the transamidation of primary amides with amines in cyclohexane at 80 °C in 5-24 hours. For favourable substrates, the reaction can be performed at temperatures as low as
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