You Searched For: Dimethylbis(t-butylcyclopentadienyl)zirconium


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Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors, Volatile Organometallics for CVD & ALD, Volatile Precursors for CVD

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Supplier: Ambeed
Description: Dimethyl-bis-(phenylethynyl)silane 98%

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors, Volatile Organometallics for CVD & ALD, Volatile Precursors for CVD

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors, Volatile Organometallics for CVD & ALD, Volatile Precursors for CVD

Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Catalog Number: (76724-942)
Supplier: Ambeed
Description: Octamethyltrisiloxane 98%


Supplier: Thermo Scientific Chemicals
Description: 5g CAS: 33010-55-8, MDL: MFCD01073803
Supplier: Strem Chemicals Inc
Description: Metallocenes, Derivatives & Cp Precursors

Supplier: Thermo Scientific Chemicals
Description: 1g CAS: 79269-71-9, MDL: MFCD01073774
Supplier: TCI America
Description: CAS Number: 107-51-7 MDL Number: MFCD00008264 Molecular Formula: C8H24O2Si3 Molecular Weight: 236.53 Purity/Analysis Method: <gt/>98.0% (GC) Form: Clear Liquid Boiling point (°C): 153 Flash Point (°C): 39 Specific Gravity (20/20): 0.82
Supplier: Adipogen
Description: Building block for synthesis. Frequently used as precursors to di-tert-butylcyclopentadienyl (Cpt) ligand in many sandwich and half sandwich complexes. Di-tert-butylcyclopentadiene reacts with excess potassium tert-butoxide in the presence of elemental selenium to yield cyclopentadienes bridged by two or three selenium atoms through one or two diselenoketal functionalities. It reacts with excess potassium tert-butoxide in the presence of elemental sulfur to yield cyclopentadienes bridged by sulfur atoms via one or two dithioketal functionalities.

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