13897-15-9 Usage
Description
4-Benzyl-2-thiazolidinethione, also known as benzylthiazolidine-2-thione, is a heterocyclic organic compound with the molecular formula C10H11NS. It features a thiazolidine ring, which is a five-membered ring containing sulfur and nitrogen atoms. 4-Benzyl-2-thiazolidinethione has attracted attention due to its diverse biological activities and potential applications in the fields of pharmaceuticals, agrochemicals, and as an antioxidant, anti-inflammatory, antimicrobial, and antitumor agent.
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-Benzyl-2-thiazolidinethione is utilized as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable component in the development of new drugs and pesticides.
Used as an Antioxidant:
4-Benzyl-2-thiazolidinethione exhibits potential as an antioxidant, which can help protect cells from damage caused by reactive oxygen species. This property makes it a candidate for use in applications where oxidative stress is a concern, such as in the prevention of chronic diseases and aging.
Used as an Anti-inflammatory Agent:
Due to its anti-inflammatory properties, 4-Benzyl-2-thiazolidinethione can be used in the treatment of inflammation-related conditions. It may help reduce inflammation and alleviate symptoms associated with various inflammatory diseases.
Used in Antimicrobial Applications:
4-Benzyl-2-thiazolidinethione has been studied for its potential use as an antimicrobial agent, showing promising activity against various microbial strains. This makes it a candidate for use in applications aimed at controlling microbial growth and preventing infections.
Used in Antitumor Applications:
4-Benzyl-2-thiazolidinethione has also been investigated for its potential as an antitumor agent, demonstrating activity against various cancer cell lines. Its use in this area could contribute to the development of new cancer treatments and therapies.
Overall, 4-Benzyl-2-thiazolidinethione is a versatile compound with a wide range of potential applications, making it a valuable asset in the fields of drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 13897-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,8,9 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13897-15:
(7*1)+(6*3)+(5*8)+(4*9)+(3*7)+(2*1)+(1*5)=129
129 % 10 = 9
So 13897-15-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11NS2/c12-10-11-9(7-13-10)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,11,12)
