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1,3,5-Trisilacyclohexane, 1,1,3,3,5,5-hexachloro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16538-69-5

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16538-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16538-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,3 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 16538-69:
(7*1)+(6*6)+(5*5)+(4*3)+(3*8)+(2*6)+(1*9)=125
125 % 10 = 5
So 16538-69-5 is a valid CAS Registry Number.

16538-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,3,3,5,5-hexachloro-1,3,5-trisilacyclohexane

1.2 Other means of identification

Product number -
Other names 1,1,3,3,5,5-Hexachlor-1,3,5-trisila-cyclohexan

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:16538-69-5 SDS

16538-69-5Downstream Products

16538-69-5Relevant academic research and scientific papers

PRODUCTION METHOD FOR LINEAR AND CYCLIC TRISILAALKANE

-

Page/Page column 5-6, (2011/04/19)

The present invention relates to a preparation method for a linear or cyclic trisilaalkane which is a substance useful in the preparation of polycarbosilane and silicon carbide precursors. Linear or cyclic trisilaalkane and organic trichlorosilane derivatives can be synthesized simultaneously and in high yield by reacting bis(chlorosily)methane having a Si—H bond, either alone or together with an organic chloride, using a quaternary organic phosphonium salt compound as a catalyst. Further, since the catalyst can be recovered after use, the present invention is very economical and is thus effective for mass-producing precursors for organic/inorganic hybrid substances.

Phosphine-Catalyzed Si-C Coupling of Bissilylmethanes: Preparation of Cyclic (Cl2SiCH2)2 and Linear Cl 2Si(CH2SiCl3)2 via Silylene and Silene Intermediates

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. 687 - 691 (2010/05/15)

Cyclic and linear carbosilanes, (Cl2SiCH2) 2 (2) and Cl2Si(CH2SiCl3) 2 (3), were produced from phosphine-catalized Si-C coupling reactions of bissilylmethanes, HCl2SiCH2SiX1X 2Cl (X1, X2 = Cl (1), X1 = H, X 2 = Cl (7), and X1 = Me, X2 = Cl (8)). The formation of compounds 2 and 3 suggested competing reaction pathways, involving dichlorosilene [CH2=SiCl2] and dichlorosilylene [:SiCl2] intermediates. Each intermediate was either proposed by the product isolation of the trimerized product (3) or confirmed by trapping experiments with 2,3-dimethylbutadiene and methylene chloride.

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