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Silanamine, 1,1,1-trimethyl-N-(trimethylsilyl)-N-[2-[(trimethylsilyl)methyl]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116458-18-5

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116458-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116458-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,4,5 and 8 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 116458-18:
(8*1)+(7*1)+(6*6)+(5*4)+(4*5)+(3*8)+(2*1)+(1*8)=125
125 % 10 = 5
So 116458-18-5 is a valid CAS Registry Number.

116458-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name orto-N,N-bis(trimethylsilyl)trimethylsilylmethyltoluidine

1.2 Other means of identification

Product number -
Other names 1,1,1,3,3,3-Hexamethyl-2-(2-trimethylsilanylmethyl-phenyl)-disilazane

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:116458-18-5 SDS

116458-18-5Downstream Products

116458-18-5Relevant academic research and scientific papers

Silylamines in organic synthesis: preparation and some reactions of N,C-dilithiosilylamines

Burns, Stephanie A.,Corriu, Robert J. P.,Huynh, Vilam,Moreau, Joel J. E.

, p. 281 - 290 (2007/10/02)

The dimetallation of some olefinic and aromatic N-trimethylsilylamines has been examined.Treatment with a two molar proportion of n-butyllithium gives organodimetallic reagents, which react with trimethylchlorosilane to give N,N,C-tris(trimethylsilyl)amines in 45 to 65percent yields.The dianonic reagent obtained from (trimethylsilyl)(allyl)amine reacts with benzoyl chloride, N,N-dimethylformamide, ethyl-2-furylcarboxylate, and benzil to give substituted pyrroles and pyridines.

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