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10543-60-9

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10543-60-9 Usage

Chemical Properties

white crystalline powder

Check Digit Verification of cas no

The CAS Registry Mumber 10543-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,4 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10543-60:
(7*1)+(6*0)+(5*5)+(4*4)+(3*3)+(2*6)+(1*0)=69
69 % 10 = 9
So 10543-60-9 is a valid CAS Registry Number.

10543-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N',N'',N'''-Tetraacetylglycoluril

1.2 Other means of identification

Product number -
Other names N,N‘,N‘‘,N‘‘‘-Tetraacetylglycoluril

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:10543-60-9 SDS

10543-60-9Relevant articles and documents

Novel Method for O-Acetylation of Cholesterol, Allobetulin, and Betulin

Arrous, Salah,Boudebouz, Imene,Bakibaev, Abdigali,Hoang, Phuoc,Parunov

, p. 482 - 484 (2019)

Primary and secondary triterpene alcohols were acetylated for the first time using tetraacetylglycoluril (TAGU). Cholesterol, allobetulin, and betulin acetates were obtained in high yields. The acetylation used p-TsOH or TFA in refluxing CHCl3. TFA was found to be an effective acetylation catalyst.

1,6-Dibenzylglycoluril for synthesis of deprotected glycoluril dimer

Stancl, Marek,Khan, Muhammad S.A.,Sindelar, Vladimir

experimental part, p. 8937 - 8941 (2011/12/01)

1,6-Dibenzylglycoluril is not accessible via classical condensation reaction between substituted urea and glyoxal. In this paper 1,6-dibenzylglycoluril was successfully prepared by alkylation of 1,6-diacetylglycoluril with benzylbromide for the first time. 1,6-Dibenzylglycoluril reacted with formaldehyde to give tetrabenzylglycoluril dimer. Deprotection of this dimer and the previously reported o-xylyleneglycoluril dimer was achieved by dissolving metal reduction, whereas propyleneglycoluril dimer was deprotected by action of potassium persulfate.

Methodes de preparation de derives nitres et nitroacetyles du glycolurile (I)

Boileau, J.,Wimmer, E.,Carail, M.,Gallo, R.

, p. 465 - 469 (2007/10/02)

A procedure for preparing nitro and nitroacetyl derivatives of glycoluril is described, starting from tetraacetylglycoluril (TAGU).The method proceeds by nitrodeacetylation and (or) hydrolysis.New compounds have been prepared : mononitrodiacetylglycoluril (MONDAGU), dinitrodiacetylglycoluril (DINDAGU) and mononitroglycoluril (MONGU).A general synthetic scheme is proposed and discussed.Some properties of the new derivatives are presented.

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