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21035-65-4

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21035-65-4 Usage

Usage

Synthetic intermediate in the production of pharmaceuticals and agrochemicals

Potential application

Treatment of type 2 diabetes as an insulin sensitizer

Additional properties

Anti-inflammatory and anti-cancer properties (in some research studies)

Safety concerns

Toxic or harmful effects on human health and the environment; caution required in handling and use

Check Digit Verification of cas no

The CAS Registry Mumber 21035-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21035-65:
(7*2)+(6*1)+(5*0)+(4*3)+(3*5)+(2*6)+(1*5)=64
64 % 10 = 4
So 21035-65-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2S/c1-6-3(8)4(9)7(2)5(6)10/h1-2H3

21035-65-4SDS

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 1,3-dimethyl-2-sulfanylideneimidazolidine-4,5-dione

1.2 Other means of identification

Product number -
Other names N,N'-Dimethylimidazolidine-2-thione-4,5-dione

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:21035-65-4 SDS

21035-65-4Relevant articles and documents

A facile protocol for the preparation of 5-alkylidene and 5-imino substituted hydantoins from N,N′-disubstituted parabanic acids

üng?ren, ?evket Hakan,Kani, Ibrahim,Günay, Ahmet

supporting information; experimental part, p. 4758 - 4762 (2012/09/07)

A convenient procedure for the preparation of various substituted (thio)hydantoins is described. The method is based on Wittig and aza-Wittig reactions of parabanic acids with phosphonium ylides. The reactions occurred both regio- and stereo-selectively.

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