90562-71-3 Usage
General Description
1-phenyl-3-(2-sulfanylethyl)thiourea is a chemical compound with the molecular formula C9H12N2S2. It is a thiourea derivative with a phenyl group and a sulfanylethyl group attached to the nitrogen atom. Thioureas are known for their diverse range of biological activities, including antiviral, antibacterial, and antifungal properties. The presence of a phenyl group in 1-phenyl-3-(2-sulfanylethyl)thiourea suggests potential biological activities, as phenyl groups are often found in drugs and other bioactive compounds. The sulfanylethyl group may also contribute to the compound's biological properties. Overall, 1-phenyl-3-(2-sulfanylethyl)thiourea has the potential to be used in medicinal or pharmaceutical applications due to its chemical structure and potential biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 90562-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,6 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 90562-71:
(7*9)+(6*0)+(5*5)+(4*6)+(3*2)+(2*7)+(1*1)=133
133 % 10 = 3
So 90562-71-3 is a valid CAS Registry Number.
90562-71-3Relevant articles and documents
A convenient method for the synthesis of 2-amino substituted aza-heterocycles from N,N′-disubstituted thioureas using TsCl/NaOH
Heinelt, Uwe,Schultheis, Daniela,J?ger, Siegfried,Lindenmaier, Marion,Pollex, Annett,Beckmann, Henning S.G.
, p. 9883 - 9888 (2007/10/03)
p-Toluenesulfonyl chloride (TsCl)/NaOH has been introduced as reagent combination for the synthesis of 2-amino-oxa- or 2-amino-thiazolidines from N-(2-hydroxyethyl)-thioureas, but its general application in heterocycle synthesis has not been investigated. In this paper the convenient and efficient synthesis of a variety of 2-amino-substituted 1-aza 3-(aza, oxo or thio) heterocycles of different substitution and ring sizes is described. The application of polymer-supported TsCl facilitates work-up and renders the reaction conditions very suitable for parallel or robot synthesis. Graphical Abstract
