107825-27-4 Usage
Description
Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-, is a chemical compound characterized by the molecular formula C13H15FNO2S. It is a thioether derivative featuring a fluorophenyl and morpholinyl substituent, which endows it with unique structural properties. As a potential drug agent, it has demonstrated promising biological activities in preclinical studies, positioning it as a candidate for further research and development within the pharmaceutical industry.
Uses
Used in Pharmaceutical Industry:
Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)is used as a potential drug agent for its demonstrated biological activities. Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)-'s unique structural features and its performance in preclinical studies make it a valuable candidate for the development of new therapeutics.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, Ethanethione, 2-(4-fluorophenyl)-1-(4-Morpholinyl)is utilized for its potential to contribute to the discovery and design of novel pharmaceuticals. Its specific structural elements, including the fluorophenyl and morpholinyl groups, offer avenues for exploration in the synthesis of new compounds with improved pharmacological properties.
Check Digit Verification of cas no
The CAS Registry Mumber 107825-27-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,8,2 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107825-27:
(8*1)+(7*0)+(6*7)+(5*8)+(4*2)+(3*5)+(2*2)+(1*7)=124
124 % 10 = 4
So 107825-27-4 is a valid CAS Registry Number.
107825-27-4Relevant articles and documents
Rapid and efficient protocol for Willgerodt–Kindler’s thioacetamides catalyzed by sulfated polyborate
Rekunge, Deelip S.,Khatri, Chetan K.,Chaturbhuj, Ganesh U.
, p. 2091 - 2095 (2017)
Abstract: A simple and efficient method for the synthesis of one-pot, three-component thioacetamides via Willgerodt–Kindler reaction was developed using a sulfated polyborate catalyst. The method described the reaction of ketones, sulfur, and secondary am
Optimum Conditions for the Willgerodt-Kindler Reaction 1: Reaction of Substituted Acetophenones. Prediction of Optimum Conditions for New Substrates by Multivariate Correlation
Carlson, Rolf,Lundstedt, Torbjoern,Shabana, Rashad
, p. 534 - 544 (2007/10/02)
Optimum conditions for the synthesis of p-substituted phenyl-acetic acid thiomorpholides by the joint action of elemental sulfur and morpholine on p-substituted acetophenones have been studied with the following substrates: p-methoxy-, p-N,N-dimethylamino
