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Dichloromethyl[2-(trichlorosilyl)ethyl]silane, with the chemical formula CH2ClSi(CH2)2SiCl3, is a colorless liquid characterized by a strong, pungent odor. It is a silane coupling agent that plays a crucial role in the synthesis of various organosilicon compounds.

15411-19-5

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15411-19-5 Usage

Uses

Used in Chemical Synthesis:
Dichloromethyl[2-(trichlorosilyl)ethyl]silane is used as a silane coupling agent for the synthesis of organosilicon compounds, contributing to the formation of these compounds' unique properties.
Used in Polymer Production:
In the Polymer Industry, dichloromethyl[2-(trichlorosilyl)ethyl]silane is used as a crosslinking agent to modify polymers, enhancing their strength and durability.
Used in the Manufacturing of Silicone Polymers:
Dichloromethyl[2-(trichlorosilyl)ethyl]silane is utilized in the production of silicone polymers, which are known for their thermal stability, flexibility, and resistance to environmental degradation.
Used in Sealants and Adhesives:
dichloromethyl[2-(trichlorosilyl)ethyl]silane is used as a component in the formulation of sealants and adhesives, providing them with improved bonding and sealing properties.
Used in Surface Coatings:
In the Coatings Industry, dichloromethyl[2-(trichlorosilyl)ethyl]silane is employed to improve the adhesion, durability, and weather resistance of surface coatings.
Safety Considerations:
Due to its high reactivity with water, strong acids, and bases, as well as its classification as a hazardous substance, dichloromethyl[2-(trichlorosilyl)ethyl]silane should be handled with care. It is essential to use it in well-ventilated areas and with appropriate personal protective equipment to ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 15411-19-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,1 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15411-19:
(7*1)+(6*5)+(5*4)+(4*1)+(3*1)+(2*1)+(1*9)=75
75 % 10 = 5
So 15411-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C3H7Cl5Si2/c1-9(4,5)2-3-10(6,7)8/h2-3H2,1H3

15411-19-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,4,4-Pentachlor-1,4-disilapentan

1.2 Other means of identification

Product number -
Other names dichloromethyl[2-(trichlorosilyl)ethyl]silane

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:15411-19-5 SDS

15411-19-5Relevant academic research and scientific papers

SILYL SUBSTITUTED 1,4-DISILACYCLOHEXANE DERIVATIVES AND PREPARATION METHOD THEREOF

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Page/Page column 4, (2011/05/08)

The present invention relates to novel 1,4-disilacyclohexane derivatives and a preparation method thereof. More particularly, the invention provides a method for preparing 1,4-disilacyclohexane derivatives with a hexagonal ring structure at high yield through double silylation of an organosilane compound and a vinyl silane compound having an unsaturated double bond using quaternary organophosphonium salts as a catalyst. According to the present invention, tris(silyl)ethanes having three silyl groups in one molecule can be prepared at the same time and the catalyst can be recovered after reaction. Thus, the method is economical and enables mass-production of 1,4-disilacyclohexane derivatives and tris(silyl)ethanes which are precursors of organic-inorganic hybrid materials.

[Bu4P]+Cl--catalyzed reactions of trichlorosilane and dichloromethylsilane with vinyltrichlorosilane: New synthetic method for 1,1,4,4-tetrachloro-2,5-bis(trichlorosilyl)-1, 4-disilacyclohexane compounds

Hong, Soon Hyun,Hyun, Sang Il,Jung, Il Nam,Han, Won-Sik,Kim, Min-Hye,Yun, Hoseop,Nam, Suk-Woo,Kang, Sang Ook

experimental part, p. 3054 - 3057 (2010/10/04)

[Bu4P]+Cl--catalyzed reactions of trichlorosilane and dichloromethylsilane with vinyltrichlorosilane gave 1,1,4, 4-tetrachloro-2,5-bis(trichlorosilyl)-1,4-disilacyclohexane (1) and 1,1,4,4-tetrachloro-2,5-bis(methyldichlor

Synthesis and Characterization of Simple α-Sila- and α,ω-Disilaalkanes: Precursors for the CVD Production of Amorphous Silicon a-SiC:H

Schmidbaur, Hubert,Doerzbach, Cornelia

, p. 1088 - 1096 (2007/10/02)

Preparative methods have been explored for the synthesis of small, volatile polysilaalkanes, which could serve as starting materials for the production of amorphous silicon a-SiC:H.High yield pathways have been developed for H3SiCH2CH2SiH3 and H3SiCH2CH2CH2SiH3.These compounds can be converted into symmetrically halogen-functional derivatives through the reactions with SnCl4 or Br2.The homologous H3SiCH2CH2SiH2CH3 has also been prepared and halogenated, starting from the corresponding vinylsilane via the hydrosilylation route.Allylsilanes were the source of the synthesis of H3SiCH2CH=CH2, CH3SiH2CH2CH=CH2, SiH2(CH2CH=CH2)2, SiH2(CH2CH2CH2SiH3)2, or HSi(CH2CH2CH2SiH3)3.Methylated derivatives are also available. - Some physical and spectroscopic properties of the new compounds have been investigated.In particular, NMR data were collected and used for an assessment of structure and isomerism. - Key words: Disilaalkanes, Silanes, Amorphous Silicon, Hydrosilylation

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