113544-16-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Methylthio-6-phenyl-4H-thiopyran-4-one is used as an active pharmaceutical ingredient for its antifungal and antimicrobial properties. Its ability to inhibit the growth of fungi and bacteria makes it a promising candidate for the development of new drugs to combat infections caused by these microorganisms.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 2-Methylthio-6-phenyl-4H-thiopyran-4-one is utilized as a lead compound for the discovery of new antimicrobial agents. Its potential to disrupt microbial cell functions and inhibit their growth offers a valuable contribution to the ongoing efforts to combat antibiotic resistance and develop novel therapeutic strategies.
Used in Antifungal Applications:
2-Methylthio-6-phenyl-4H-thiopyran-4-one is employed as an antifungal agent, targeting the inhibition of fungal growth and proliferation. Its application in this area is crucial for the development of treatments for various fungal infections, which can be particularly challenging to manage due to the emergence of drug-resistant strains.
Used in Drug Development Research:
2-Methylthio-6-phenyl-4H-thiopyran-4-one serves as a valuable compound in drug development research, where its unique structure and bioactivity are explored for the creation of new pharmaceuticals. Its potential to be modified and optimized for specific therapeutic applications makes it an attractive target for further investigation and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 113544-16-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113544-16:
(8*1)+(7*1)+(6*3)+(5*5)+(4*4)+(3*4)+(2*1)+(1*6)=94
94 % 10 = 4
So 113544-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C12H10OS2/c1-14-12-8-10(13)7-11(15-12)9-5-3-2-4-6-9/h2-8H,1H3
113544-16-4Relevant academic research and scientific papers
INTRAMOLECULAR MICHAEL AND ANTI-MICHAEL ADDITIONS OF THIOLATE TO CONJUGATED ACETYLENIC KETONES
Rudorf, Wolf-Dieter,Schwarz, Ralf
, p. 4267 - 4270 (2007/10/02)
The reaction of acetylenic ketones 1 with carbon disulfide in the basic system sodium hydride/dimethylformamide and subsequent intramolecular cyclization to 4H-thiopyran-4-ones 3 and 3(2H)-thiophenones 4 are reported.
