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Silane, (1,1-dimethylethoxy)triethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18132-83-7

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18132-83-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18132-83-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,3 and 2 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 18132-83:
(7*1)+(6*8)+(5*1)+(4*3)+(3*2)+(2*8)+(1*3)=97
97 % 10 = 7
So 18132-83-7 is a valid CAS Registry Number.

18132-83-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl-tert-butoxy-silane

1.2 Other means of identification

Product number -
Other names Triaethyl-tert-butoxy-silan

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:18132-83-7 SDS

18132-83-7Relevant academic research and scientific papers

Alcoholysis Equilibria of Triethylalkoxysilanes Catalyzed by Iodine or Iodine Monobromide

Ito, Katsuko,Ibaraki, Takeshi

, p. 2973 - 2975 (2007/10/02)

The equilibrium constants K of alcoholysis of triethylalkoxysilanes were determined at 20 degC and 40 degC.Iodine monobromide was used to promote the reactions associated with the tertiary alkoxyl groups, while the other reactions proceeded in the presence of iodine.The K values of the reaction systems with ethoxyl or propoxyl-primary, secondary, and tertiary alkoxyl pairs were 1 or above, about 0.5, and about 0.05, respectively.These values reflect the extent of the binding abilities of the alkoxyl groups to silicon, which is in the expected order of primary>secondary>tertiary alkoxyl groups.A mechanism is postulated for the reaction which involves participation by the iodine or iodine monobromide.

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