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Triethylpentoxysilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14629-52-8

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14629-52-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14629-52-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,2 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 14629-52:
(7*1)+(6*4)+(5*6)+(4*2)+(3*9)+(2*5)+(1*2)=108
108 % 10 = 8
So 14629-52-8 is a valid CAS Registry Number.

14629-52-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name triethyl(pentoxy)silane

1.2 Other means of identification

Product number -
Other names Triaethyl-pentyloxy-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:14629-52-8 SDS

14629-52-8Relevant academic research and scientific papers

Hydrosilylation of epoxides catalyzed by a cationic η1- silane iridium(iii) complex

Park, Sehoon,Brookhart, Maurice

supporting information; experimental part, p. 3643 - 3645 (2011/05/04)

Cationic silane complex 2, catalyzes the hydrosilylation of epoxides and cyclic ethers to give the silyl-protected alcohols, regioselectively. A mechanistic study shows that the epoxide undergoes isomerization to the ketone, followed by hydrosilylation.

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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