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1,2,3-Trisilacyclopent-4-ene, 1,1,2,2,3,3-hexamethyl-4,5-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69093-08-9

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69093-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69093-08-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,9 and 3 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 69093-08:
(7*6)+(6*9)+(5*0)+(4*9)+(3*3)+(2*0)+(1*8)=149
149 % 10 = 9
So 69093-08-9 is a valid CAS Registry Number.

69093-08-9SDS

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 1,1,2,2,3,3-hexamethyl-4,5-diphenyl-1,2,3-trisilacyclopent-4-ene

1.2 Other means of identification

Product number -
Other names 1,1,2,2,3,3-hexamethyl-4,5-diphenyl-2,3-dihydro-1H-[1,2,3]trisilole

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:69093-08-9 SDS

69093-08-9Relevant academic research and scientific papers

An Electroreductive Approach to Radical Silylation via the Activation of Strong Si-Cl Bond

Lu, Lingxiang,Siu, Juno C.,Lai, Yihuan,Lin, Song

, p. 21272 - 21278 (2020/12/21)

The construction of C(sp3)-Si bonds is important in synthetic, medicinal, and materials chemistry. In this context, reactions mediated by silyl radicals have become increasingly attractive but methods for accessing these intermediates remain limited. We present a new strategy for silyl radical generation via electroreduction of readily available chlorosilanes. At highly biased potentials, electrochemistry grants access to silyl radicals through energetically uphill reductive cleavage of strong Si-Cl bonds. This strategy proved to be general in various alkene silylation reactions including disilylation, hydrosilylation, and allylic silylation under simple and transition-metal-free conditions.

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