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methoxy(2-methylpropyl)bis(propan-2-yloxy)silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

118337-13-6

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118337-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118337-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,3 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 118337-13:
(8*1)+(7*1)+(6*8)+(5*3)+(4*3)+(3*7)+(2*1)+(1*3)=116
116 % 10 = 6
So 118337-13-6 is a valid CAS Registry Number.

118337-13-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methoxy-(2-methylpropyl)-di(propan-2-yloxy)silane

1.2 Other means of identification

Product number -
Other names -

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:118337-13-6 SDS

118337-13-6Downstream Products

118337-13-6Relevant academic research and scientific papers

Contributions to the chemistry of silicon-sulphur compounds LVI. The imidazole catalyzed alcoholysis of the isosteric isobutyl(isopropoxy)silanethiols i-Bun(i-PrO)3-nSiSH (n = 0-3)

Pikies, J.,Wojnowski W.

, p. 305 - 312 (1990)

The kinetics of the imidazole-catalyzed alcoholysis of the isosteric silanethiols i-Bun(i-PrO)3-nSiSH (I) with n = 0-3 in benzene and acetonitrile have been investigated.The alcoholysis of Si-S bond in I is generally first order with respect to both the silanethiol and the catalyst.At low alcohol concentrations the order with respect to alcohol tends to be zero.A mechanism involving an attack of a nucleophilic catalyst on silicon in I in the rate-determining step is proposed.In MeCN solution the reactivities of silanethiols decrease in the sequence i-Bu(i-PrO)2SiSH > i-Bu2(i-PrO)SiSH > (i-PrO)3SiSH > i-Bu3SiSH.The anomeric effect seems to determine the conformations and the reactivities of these silanethiols.

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