5316-79-0

Usage

Uses

Used in Organic Synthesis:
3,4-Dimethyl-4-thiazoline-2-thione is utilized as a reagent in organic synthesis, playing a crucial role in the formation of various complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 3,4-Dimethyl-4-thiazoline-2-thione serves as an intermediate. Its unique structure contributes to the development of new drugs, enhancing the range of treatments available for various health conditions.
Used in Agrochemicals:
3,4-Dimethyl-4-thiazoline-2-thione is also employed as an intermediate in the production of agrochemicals, which are essential for developing pesticides and other agricultural products to ensure crop protection and yield enhancement.
Used in Material Development:
3,4-Dimethyl-4-thiazoline-2-thione has been used in the development of materials for diverse applications. Its incorporation in the production of polymers and coatings highlights its potential to improve material properties and contribute to the advancement of various industries.
Overall, 3,4-Dimethyl-4-thiazoline-2-thione is a multifaceted chemical with a broad spectrum of applications across different sectors, including organic synthesis, pharmaceuticals, agrochemicals, and material development. Its antimicrobial and antifungal properties further expand its potential uses, making it a valuable component in the creation of innovative products and solutions.

InChI:InChI=1/C5H7NS2/c1-4-3-8-5(7)6(4)2/h3H,1-2H3

Upstream product

• 55019-79-9 4-methyl-3-phenethyl-3H-thiazole-2-thione 
• 78-95-5 chloroacetone 
• 21160-95-2 methyl-dithiocarbamic acid; methylamine salt 
• 24300-70-7 3,4-dimethylthiazolinium iodide 
• 39713-76-3 methyl dithiocarbamic acid triethylammonium 
• 75-15-0 carbon disulfide 
• 74-89-5 methylamine 
• 33167-53-2 3,4-dimethyl-2-(methylthio)-1,3-thiazol-3-ium iodide 
• 19975-65-6 4-hydroxy-3,4-dimethyl-thiazolidine-2-thione 

Downstream Products

• 894794-02-6 3,4-dimethyl-2-thioxo-2,3-dihydro-1,3-thiazole-5-carbaldehyde 
• 55379-27-6 benzyl-(3,4-dimethyl-3H-thiazol-2-ylidene)-amine 

Relevant academic research and scientific papers

Synthesis of new rhodacyanines analogous to MKT-077 under microwave irradiation

We report here a synthesis of a new rhodacyanines 7X analogous to MKT-077 with quantitative yield using as starting material the thiazolinethione 1. Merocyanines 4 and their tosylates 5 have been prepared as intermediates for this class of compounds. The reactions leading to rhodacyanine 7X have been studied under microwave irradiation. Copyright Taylor & Francis Group, LLC.

Chemical and electrochemical investigations on thiazolium salts: A route to powerful donors in the dithiadiazafulvalene series

Thiazolium salts have been investigated, chemically and electrochemically, in order to access to the redox properties of dithiadiazafulvalenes (DTDAF). As these donor molecules are oxygen-sensitive, it is more advisable to isolate them in their oxidized f

The reaction of 3-methylthiazolium derivatives with superoxide

3-Methylbenzothiazolium salts were allowed to react with superoxide to afford dimeric bis[o-(N-formyl-N-methylamino)phenyl]disulfides and 3-methyl-2-benzothiazolones. The reaction was applied to monocyclic thiazolium salts, and novel ten-membered ring com

REACTION OF N-ALKYLTHIAZOLIUM HALIDES, INCLUDING THIAMINE, WITH SUPEROXIDE ION. CHEMISTRY AND BIOLOGICAL IMPLICATIONS.

N-alkylthiazolium halides are transformed by KO2 into the corresponding thiazolin-2-ones and thiazolin-2-thiones; the same reactions occur with thiamine, whose thiazolin-2-one pyrophosphate has been reported to be a strong inhibitor of pyruvic dehydrogenase.