5338-82-9 Usage
Uses
Used in Pharmaceutical Research:
(5Z)-4-phenyl-5-(phenylimino)-1,2,4-dithiazolidin-3-one is used as a therapeutic agent for treating type 2 diabetes. It aids in reducing insulin resistance and effectively regulates blood sugar levels, making it a promising compound for diabetes management.
Used in Cardiovascular Disease Treatment:
In the field of cardiovascular disease treatment, (5Z)-4-phenyl-5-(phenylimino)-1,2,4-dithiazolidin-3-one is utilized for its anti-inflammatory and antioxidant properties. These characteristics contribute to its potential value in addressing and mitigating the effects of cardiovascular conditions.
Used in Anti-Inflammatory Applications:
(5Z)-4-phenyl-5-(phenylimino)-1,2,4-dithiazolidin-3-one is employed as an anti-inflammatory agent, leveraging its capacity to combat inflammation and related conditions, thus providing relief and support in the treatment process.
Used in Antimicrobial and Anti-Fungal Applications:
Within the antimicrobial and antifungal sectors, (5Z)-4-phenyl-5-(phenylimino)-1,2,4-dithiazolidin-3-one is used for its demonstrated activities against various microorganisms. This makes it a versatile compound in the development of treatments for a range of infections and fungal conditions.
Used in Organic Synthesis:
In the chemical industry, (5Z)-4-phenyl-5-(phenylimino)-1,2,4-dithiazolidin-3-one serves as a key intermediate in organic synthesis, facilitating the creation of a variety of complex molecules and compounds with diverse applications in science and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 5338-82-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5338-82:
(6*5)+(5*3)+(4*3)+(3*8)+(2*8)+(1*2)=99
99 % 10 = 9
So 5338-82-9 is a valid CAS Registry Number.
5338-82-9Relevant academic research and scientific papers
Novel Heterocyclization of 4-Phenylthiosemicarbazones and Related Compounds with Chlorocarbonylsulfenyl Chloride
Kabashima, Shigeru,Okawara, Tadashi,Yamasaki, Tetsuo,Furukawa, Mitsuru
, p. 1957 - 1960 (2007/10/02)
Chlorocarbonylsulfenyl chloride was allowed to react with 1-alkylidene-4-phenylthiosemicarbazones in the presence of triethylamine to give 1,2,4-triazolines, whereas with 1-arylidene-4-phenylthiosemicarbazones to afford 1,2,4-dithiazolidines.Treatment of diarylidenethiocarbohydrazides and diarylidenaminoguanidines with chlorocarbonylsulfenyl chloride under similar conditions gave 1,2,4-dithiazolidines and 1,2,4-thiadiazolidines, respectively.
Synthesis of Mustard Oil Oxides with Different Substituents
Tittelbach, Franz
, p. 180 - 190 (2007/10/02)
Treatment of N-alkyl-N'-aryl-thioureas with chlorocarbonylsulfenyl chloride leads to 2-alkyl-4-aryl-3-thiono-1,2,4-thiadiazolidin-3-ones (4).Isomerization of 4 takes place in the presence of strong acids to give 5-alkylimino-4-aryl-1,2,4-dithiazolidin-3-o
