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52726-86-0

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52726-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52726-86-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 52726-86:
(7*5)+(6*2)+(5*7)+(4*2)+(3*6)+(2*8)+(1*6)=130
130 % 10 = 0
So 52726-86-0 is a valid CAS Registry Number.

52726-86-0SDS

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 N-trimethylsilyl-4-trimethylsilyloxyaniline

1.2 Other means of identification

Product number -
Other names N-(Trimethylsilyl)-N-(4-[(trimethylsilyl)oxy]phenyl)amine

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:52726-86-0 SDS

52726-86-0Relevant articles and documents

A simple and efficient room temperature silylation of diverse functional groups with hexamethyldisilazane using CeO2 nanoparticles as solid catalysts

Anbu, Nagaraj,Vijayan, Chellappa,Dhakshinamoorthy, Amarajothi

, (2019/06/08)

In this study, a mild and efficient method is developed for the silylation of diverse functional groups using CeO2 nanoparticles (n-CeO2) as solid catalysts with hexamethyldisilazane (HMDS) as silylating agent at room temperature. Alcohols, phenols and acids are silylated to their respective silyl derivatives with faster reaction rate while amines and thiols required relatively longer reaction time. Moreover, the solid catalyst is easily be separated from the reaction mixture and recycled more than five times without any obvious decay in its activity. Powder X-ray diffraction (XRD), transmission electron microscope (TEM), UV–vis diffuse reflectance spectra (UV-DRS) and Raman analyses revealed identical structural integrity, particle size, absorption edge and valence state for the reused solid compared to the fresh solid catalyst.

A study of ortho- and para-siloxyanilines for the synthesis of mono-, bi-, and tetra-nuclear early transition metal-imido complexes

Benito,Arévalo, Silvia,De Jesús,De La Mata,Flores,Gómez

, p. 42 - 48 (2007/10/03)

The siloxyanilines o-Me3SiOC6H4NH2 (1) and p-RMe2SiOC6H4NH2 (R = H (2); R = Me (3)), and their N-silylated derivatives p-Me3SiOC6H4NHS

SELECTIVE N-MONOMETHYLATION OF PRIMARY AMINES via N-TRIALKYLSILYL-LITHIOAMINES

Calverley, Martin J.

, p. 601 - 610 (2007/10/02)

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