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18246-71-4

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18246-71-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18246-71-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18246-71:
(7*1)+(6*8)+(5*2)+(4*4)+(3*6)+(2*7)+(1*1)=114
114 % 10 = 4
So 18246-71-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H20O2Si/c1-5-7-8-10-11(3,4)9-6-2/h5-8H2,1-4H3

18246-71-4SDS

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 Butoxy(ethoxy)dimethylsilane

1.2 Other means of identification

Product number -
Other names 2-Ethoxy-4,6-bis-(trichlormethyl)-s-triazin

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:18246-71-4 SDS

18246-71-4Relevant articles and documents

Iodine- or Iodine Monobromide-Catalyzed Alkoxy-Alkoxy Exchange Reactions of Alkylalkoxysilanes: Formation of the Catalyst-Alkoxysilane Complexes and the Reaction Mechanism

Ito, Katsuko,Ibaraki, Takeshi

, p. 2853 - 2858 (2007/10/02)

The formation of charge-transfer complexes of iodine and of iodine monobromide with alcohols and alkoxysilanes has been established spectroscopically, and the formation constants of iodine-ethoxytriethylsilane and iodine-diethoxydimethylsilane complexes has been determined as 0.55+/-0.01 and 0.61+/-0.02, respectively.On the basis of these observations and the kinetic information recently reported, the previously proposed mechanism for the iodine or iodine monobromide catalyzed alkoxy-alkoxy exchange reactions of alkoxysilanes is dicussed afresh.It has been confirmed that a mechanism involving a four-centered transition state containing a CT-complex is most favorable.

The Disproportionation of Dimethyldialkoxysilanes Catalyzed by Iodine Monobromide

Ibaraki, Takeshi,Ito, Katsuko

, p. 3235 - 3236 (2007/10/02)

Iodine monobromide is an extremely effective catalyst for the redistribution of alkoxyl groups on silicon atoms in dimethyldialkoxysilanes.The equilibrium constants of these reactions were determined at 40 deg C by means of gas chromatography.Assuming that the reaction intermediate is the dative form of a dimethyldialkoxysilaneiodine monobromide complex, a mechanism of the reaction was proposed.

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