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CHLORODIMETHYLOCTYLSILANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18162-84-0

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18162-84-0 Usage

Chemical Properties

CLEAR COLOURLESS LIQUID

Check Digit Verification of cas no

The CAS Registry Mumber 18162-84-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18162-84:
(7*1)+(6*8)+(5*1)+(4*6)+(3*2)+(2*8)+(1*4)=110
110 % 10 = 0
So 18162-84-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H23ClSi/c1-4-5-6-7-8-9-10-12(2,3)11/h4-10H2,1-3H3

18162-84-0 Well-known Company Product Price

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  • Alfa Aesar

  • (L16564)  Chlorodimethyl-n-octylsilane, 97%   

  • 18162-84-0

  • 5g

  • 231.0CNY

  • Detail
  • Alfa Aesar

  • (L16564)  Chlorodimethyl-n-octylsilane, 97%   

  • 18162-84-0

  • 25g

  • 923.0CNY

  • Detail
  • Aldrich

  • (246859)  Chloro(dimethyl)octylsilane  97%

  • 18162-84-0

  • 246859-25G

  • 1,353.69CNY

  • Detail

18162-84-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-dimethyl-octylsilane

1.2 Other means of identification

Product number -
Other names n-Octyldimethylchlorosilane

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:18162-84-0 SDS

18162-84-0Relevant academic research and scientific papers

A General and Selective Synthesis of Methylmonochlorosilanes from Di-, Tri-, and Tetrachlorosilanes

Naganawa, Yuki,Nakajima, Yumiko,Sakamoto, Kei

supporting information, p. 601 - 606 (2021/01/13)

Direct catalytic transformation of chlorosilanes into organosilicon compounds remains challenging due to difficulty in cleaving the strong Si-Cl bond(s). We herein report the palladium-catalyzed cross-coupling reaction of chlorosilanes with organoaluminum reagents. A combination of [Pd(C3H5)Cl]2 and DavePhos ligand catalyzed the selective methylation of various dichlorosilanes 1, trichlorosilanes 5, and tetrachlorosilane 6 to give the corresponding monochlorosilanes.

Nickel-Catalyzed Selective Cross-Coupling of Chlorosilanes with Organoaluminum Reagents

Naganawa, Yuki,Guo, Haiqing,Sakamoto, Kei,Nakajima, Yumiko

, p. 3756 - 3759 (2019/09/12)

Nickel-catalyzed cross-coupling reactions of chlorosilanes with organoaluminum reagents were developed. An electron-rich Ni(0)/PCy3 complex was found to be an effective catalyst for the desired transformation. The reaction of dichlorosilanes 1 proceeded to give the corresponding monosubstituted products 2. Trichlorosilanes 4 underwent selective double substitution to furnish the corresponding monochlorosilanes 2. Overall, the selective synthesis of a series of alkylmonochlorosilanes 2 from di- and trichlorosilanes was achieved using the present catalytic systems.

Waste-free and efficient hydrosilylation of olefins

Pandarus, Valerica,Ciriminna, Rosaria,Gingras, Geneviève,Béland, Fran?ois,Kaliaguine, Serge,Pagliaro, Mario

, p. 129 - 140 (2019/01/11)

High purity silicone precursors can now be synthesized by hydrosilylation of solvent-free olefins catalyzed by a highly stable and active glass hybrid catalyst consisting of mesoporous organosilica microspheres doped with Pt nanoparticles. These findings open the door to the sustainable manufacture of silicone and a way to further reduce the amount of platinum in silicones, which are ubiquitous advanced polymers with multiple uses and applications.

Hydrosilylation of alkenes catalyzed by Fe powder

Yang, Xiaoling,Bai, Ying,Li, Jiayun,Dai, Zinan,Peng, Jiajian

, p. 1 - 4 (2019/02/01)

A novel iron-catalyzed hydrosilylation of alkenes process under solvent-free conditions has been reported. The influence of the amount of Fe catalyst, reaction temperature and various alkenes and silanes on the hydrosilylation were investigated. High yields of adduct were obtained in the hydrosilylation of octene with MeCl2H, Me2ClSiH and Ph2SiH2 by using 10 mol% iron powder as a signal catalyst.

METHOD OF PRODUCING ORGANOHALOSILANES

-

Paragraph 0084, (2016/09/22)

A method for producing an organohalosilanes comprising reacting an organic compound comprising a halogen-substituted or unsubstituted alkane, a halogen-substituted or unsubstituted alkene, or an aromatic compound and at least one hydridohalosilane of formula RnSiHmX4-m-n, wherein each R is independently C-1 -C-1 4 hydrocarbyl or C-1 -C-1 4 hologen-substituted hydrocarbyl, X is fluoro, chloro, bromo, or iodo, n is 0, 1, or 2, m is 1, 2 or 3, and m+n=1, 2 or 3, in the presence of a heterogeneous catalyst comprising an oxide of one or more of the elements Sc, Y, Ti, Zr, Hf, B, Al, Ga, In, C, Si, Ge, Sn, or Pb, at a temperature greater than 100 °C, and at a pressure of at least 690 kPa, to produce a crude reaction product comprising the organohalosilane.

Hydrosilylation of alkenes catalyzed by rhodium with polyethylene glycol-based ionic liquids as ligands

Xu, Yisong,Bai, Ying,Peng, Jiajian,Li, Jiayun,Xiao, Wenjun,Lai, Guoqiao

, p. 59 - 63 (2014/06/09)

A series of polyethylene glycol-functionalized imidazolium ionic liquids has been prepared and characterized. These ionic liquids have been successfully applied in the hydrosilylation of alkenes catalyzed by rhodium complexes. The effects of the length of the polyether chain, the amount of ionic liquid, and the reaction temperature on the catalytic performance of hydrosilylation have been investigated. Furthermore, the catalytic system has been tested for the hydrosilylation of different alkenes with triethoxysilane. The new catalytic system exhibits both excellent catalytic activity and selectivity under low-temperature conditions. The catalyst system could be recycled five times with slightly deactivation.

Synthesis of Certain Cyclic Silanes

House, Herbert O.,Hrabie, Joseph A.,Narasimhan, S. Lakshmi

, p. 124 - 127 (2007/10/02)

The chlorotrialkylsilanes 21-24 have been synthesized as precursors to potential steric blocking groups for alkanes and cycloalkanes.Reaction of these chlorosilanes with one of the organometallic reagents methyllithium, methylmagnesium chloride, n-octylmagnesium bromide, or p-chlorobenzylmagnesium chloride formed the silanes 25-34.

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