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DI(CYCLOPENTADIENYL)DIMETHYLSILANE, with the chemical formula (C5H4Si(CH3)2)2, is a colorless liquid characterized by a strong odor and high flammability. DI(CYCLOPENTADIENYL)DIMETHYLSILANE serves as a versatile reagent in organic synthesis and a precursor for silicon-containing polymers and materials.

18053-74-2

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18053-74-2 Usage

Uses

Used in Organic Synthesis:
DI(CYCLOPENTADIENYL)DIMETHYLSILANE is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of a wide range of silicon-containing compounds.
Used in Silicon-Containing Polymers and Materials Production:
DI(CYCLOPENTADIENYL)DIMETHYLSILANE is utilized as a precursor in the production of silicon-containing polymers and materials, which have applications in various industries due to their unique properties.
Used in Chemical Vapor Deposition Processes:
DI(CYCLOPENTADIENYL)DIMETHYLSILANE is employed as a source of silicon in chemical vapor deposition processes, where it helps in depositing thin films of silicon-containing materials for use in different applications.
Used in Semiconductor Industry:
In the semiconductor industry, DI(CYCLOPENTADIENYL)DIMETHYLSILANE is used for the fabrication of electronic devices, playing a crucial role in the development of advanced technologies.
Safety Precautions:
Given its hazardous nature, caution should be exercised when handling and storing DI(CYCLOPENTADIENYL)DIMETHYLSILANE to prevent accidents and ensure safe usage.

Check Digit Verification of cas no

The CAS Registry Mumber 18053-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,5 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18053-74:
(7*1)+(6*8)+(5*0)+(4*5)+(3*3)+(2*7)+(1*4)=102
102 % 10 = 2
So 18053-74-2 is a valid CAS Registry Number.

18053-74-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name bis-(cyclopentadienyl)dimethylsilane

1.2 Other means of identification

Product number -
Other names dicyclopentadienyldimethylsilane

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:18053-74-2 SDS

18053-74-2Relevant academic research and scientific papers

Bridging effect in the polymerisations of 1,3-butadiene catalysed by Me2SiCp2TiCl2/MAO catalyst. Polymerisation activity and stereospecificity

Miyazawa, Akira,Suzuki, Yasuzo

, p. 503 - 505 (2007/10/03)

A combination of dimethylsilylene-bridged bis- cyclopentadienyltitanium dichloride and methylaluminoxane showed high catalytic performance toward the polymerisation of 1,3-butadine.

Synthesis and reactivity of new mixed dicyclopentadienyl Group 4 metal complexes with the doubly bridged bis(dimethylsilanediyl)-cyclopentadiene-(η5-cyclopentadienyl) ligand

Gomez-Garcia, Roberto,Royo, Pascual

, p. 86 - 93 (2007/10/03)

The monocyclopentadienyl titanium complex [Ti{(C5H4)(SiMe2)2(η 5-C5H3)} Cl3] 3 and the dichloro mixed dicyclopentadienyl Group 4 metal complexes [M(η5-C5R5){(C5H 4)(SiMe2)2(η5-C 5H3)} Cl2] (R=H; M=Ti 4, Zr 5, Hf 6; R=Me; M=Ti 7) containing the doubly bridged bis(dimethylsilanediyl)-cyclopentadiene-(η5-cyclopentadienyl) ligand were prepared in high yields by reaction of the monolithium salt Li[(C5H4)(SiMe2)2(C 5H3)] 2 with equimolar amounts of TiCl4 or the monocyclopentadienyl complexes [Cp′MCl3], respectively. Reactions of the chloro complexes with various alkylating agents afforded the chloroalkyl [M(η5-C5H5){(C5H 4)(SiMe2)2(η5-C 5H3)}ClR] (M=Ti; R=Me 8, Et 9; M=Zr, R=Me 10, Et 11, CH2Ph 12; M=Hf, R=CH2Ph 13) and dialkyl [M(η5-C5R5){(C5H 4)(SiMe2)2(η5-C 5H3)}Me2] (M=Ti; R=H 14, Me 15; M=Zr; R=H 16, compounds. Formation of the heterodinuclear complex [Zr(η5-C5H5)Cl2(η 5-C5H3)(SiMe2) 2(η5-C5H3)Ti(NMe 2)3] 17 with amine elimination was observed by 1H-NMR spectroscopy when complex 5 was reacted with Ti(NMe2)4. The catalytic activity of compounds 3-5 for ethylene polymerization has been studied using MAO as cocatalyst.

6,6-DIMETHYL-6-SILAFULVENE. GENERATION AND TRAPPING REACTIONS

Nakadaira, Yasuhiro,Sakaba, Hiroyuki,Sakurai, Hideki

, p. 1071 - 1074 (2007/10/02)

6,6-Dimethyl-6-silafulvene generated from (allyl)(cyclopentadienyl)-dimethylsilane reacts with a trapping reagent such as methanol, benzaldehyde, and benzophenone to give (cyclopentadienyl)(methoxy)dimethylsilane, 6-phenylfulvene, and 6,6-diphenylfulvene, respectively.Without a trapping reagent, the silafulvene undergoes dimerization.

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