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3429-74-1

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3429-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3429-74-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,2 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3429-74:
(6*3)+(5*4)+(4*2)+(3*9)+(2*7)+(1*4)=91
91 % 10 = 1
So 3429-74-1 is a valid CAS Registry Number.

3429-74-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tetra(octyl)silane

1.2 Other means of identification

Product number -
Other names tetraoctyl-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:3429-74-1 SDS

3429-74-1Downstream Products

3429-74-1Relevant articles and documents

Formal SiH4 chemistry using stable and easy-to-handle surrogates

Simonneau, Antoine,Oestreich, Martin

, p. 816 - 822 (2015/10/05)

Monosilane (SiH4) is far less well behaved than its carbon analogue methane (CH4). It is a colourless gas that is industrially relevant as a source of elemental silicon, but its pyrophoric and explosive nature makes its handling and use challenging. Consequently, synthetic applications of SiH4 in academic laboratories are extremely rare and methodologies based on SiH4 are underdeveloped. Safe and controlled alternatives to the substituent redistribution approaches of hydrosilanes are desirable and cyclohexa-2,5-dien-1-ylsilanes where the cyclohexa-1,4-diene units serve as placeholders for the hydrogen atoms have been identified as potent surrogates of SiH4. We disclose here that the commercially available Lewis acid tris(pentafluorophenyl)borane, B(C6F5)3, is able to promote the release of the Si-H bond catalytically while subsequently enabling the hydrosilylation of C-C multiple bonds in the same pot. The net reactions are transition-metal-free transfer hydrosilylations with SiH4 as a building block for the preparation of various hydrosilanes.

Preparation of tetraalkylsilanes from trichloromethylsilane and trioctylaluminum

Sabourin,Onopchenko

, p. 3691 - 3696 (2007/10/02)

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