90562-71-3 Usage
Uses
Used in Pharmaceutical Industry:
1-phenyl-3-(2-sulfanylethyl)thiourea is used as a potential therapeutic agent for its diverse biological activities, including antiviral, antibacterial, and antifungal properties. The presence of the phenyl and sulfanylethyl groups may enhance its efficacy in treating various infections and diseases.
Used in Medicinal Chemistry Research:
1-phenyl-3-(2-sulfanylethyl)thiourea serves as a valuable compound in medicinal chemistry research for the development of new drugs. Its unique chemical structure and potential biological activities make it a promising candidate for further investigation and optimization to improve its therapeutic potential.
Used in Drug Design and Synthesis:
1-phenyl-3-(2-sulfanylethyl)thiourea is utilized in drug design and synthesis processes to create novel compounds with improved pharmacological properties. Its chemical structure can be modified to explore new therapeutic applications and enhance its 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 academic research and scientific papers
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
