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Dimethylsilylbis(tetramethylcyclopentadienyl)zirconium dichloride, commonly known as zirconocene dichloride, is a metalorganic compound characterized by a zirconium atom bonded to two cyclopentadienyl rings and two chloride atoms. It is a type of zirconocene complex that exhibits unique structural and reactivity features, making it a valuable chemical in the realm of organometallic chemistry and catalysis.

100516-64-1

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100516-64-1 Usage

Uses

Used in Organic Synthesis:
Zirconocene dichloride is utilized as a catalyst in various organic synthesis processes, including olefin polymerization, esterification, and alkylation reactions. Its effectiveness in these transformations is attributed to its unique structure and reactivity.
Used in Polymer Production:
In the polymer industry, zirconocene dichloride is employed in the production of high-quality polymers. Its catalytic properties contribute to the synthesis of polymers with desirable characteristics, such as improved strength, flexibility, and thermal stability.
Used in Specialty Chemicals Synthesis:
Zirconocene dichloride also serves as a catalyst in the synthesis of specialty chemicals. Its application in this field allows for the production of chemicals with specific properties required for various applications, such as pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 100516-64-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,5,1 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100516-64:
(8*1)+(7*0)+(6*0)+(5*5)+(4*1)+(3*6)+(2*6)+(1*4)=71
71 % 10 = 1
So 100516-64-1 is a valid CAS Registry Number.

100516-64-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl-λ<sup>3</sup>-silane,1,2,3,5-tetramethylcyclopenta-1,3-diene,zirconium(4+),dichloride

1.2 Other means of identification

Product number -
Other names Dimethylsilyl bis(tetramethylcyclopentadienyl)zirconium dichloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:100516-64-1 SDS

100516-64-1Relevant academic research and scientific papers

Unexpected P-Si or P-C bond cleavage in the reaction of Li2[(C5Me4)SiMe2PR] (R = Cyclohexyl, 2,4,6-Me3C6H2) and Li[(C5H4)CMe2PHR] (R = Ph, t

Koch,Blaurock,Somoza,Voigt,Kirmse,Hey-Hawkins

, p. 2556 - 2563 (2008/10/08)

The (phosphinosilyl)cyclopentadiene 1-SiMe2PHMes-2,3,4,5-Me4C5H, prepared from 1-SiMe2-Cl-2,3,4,5-Me4C5H and LiPHMes (Mes = 2,4,6-Me3C6H2), reacts with MeLi

Metal Complexes with Bridged Permethylated Cyclopentadienyl Ligands

Jutzi, Peter,Dickbreder, Reiner

, p. 1750 - 1754 (2007/10/02)

The preparation of the permethylated silyl-bridged dicyclopentadienyl ligands Me2Si(Me4C5H)2 (1) and C2H4(Me2Si(Me4C5H))2 (2) is reported.Reaction of dimetalated 1 with TiCl4 and ZrCl4 yielded the corresponding metallocenophane dihalides 3 and 4, while treatment of the dilithio derivative of 2 with GeCl2 * dioxane, SnCl2, and FeCl2 yielded the bridged metallocenes 5, 6, and 7.

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