21885-29-0

Usage

Uses

Used in Pharmaceutical Industry:
2,4-dimethyl-2,4-dihydro-3H-1,2,4-triazole-3-thione is used as a pharmaceutical agent for its antibacterial, antifungal, and potential therapeutic properties in treating certain diseases. Its unique structure and reactivity make it a promising candidate for drug development.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-dimethyl-2,4-dihydro-3H-1,2,4-triazole-3-thione is utilized as an active ingredient in fungicides, herbicides, and other crop protection products. Its broad-spectrum activity against various pathogens and pests contributes to enhanced crop yield and quality.
Used in Materials Science:
2,4-dimethyl-2,4-dihydro-3H-1,2,4-triazole-3-thione serves as an intermediate in the synthesis of various compounds in materials science. Its versatile reactivity allows for the development of new materials with improved properties, such as enhanced stability, durability, or specific functional characteristics.
Overall, 2,4-dimethyl-2,4-dihydro-3H-1,2,4-triazole-3-thione is a multifaceted compound with a wide range of applications in different industries, showcasing its potential for further research and development.

Upstream product

• 6621-75-6 2,4-dimethylthiosemicarbazide 
• 122-51-0 orthoformic acid triethyl ester 
• 1438388-63-6 1,4-dimethyl-4H-1,2,4-triazol-1-ium methyl sulfate 

Relevant academic research and scientific papers

Synthesis and crystal structures of new 1,4-disubstituted 1,2,4-triazoline-5-thiones

Introduction of sulfur into the 5-position of 1,4-disubstituted quaternary 1,2,4-triazolium salts (1-9; Cl, Br, I, BF4, PF6, CH3OSO3 were used as anions) by two methods was investigated. The syntheses of nine 1,

A new synthetic method for substituted 2,4-dihydro-3H-1,2,4-triazol-3-ones and 3-thiones via 1,4-dialkyl-5-phenylthio-1H-1,2,4-triazolium salts

Novel 2,4-di- and 2,4,5-trialkyl-2,4-dihydro-3H-1,2,4-triazol-3-ones and 2,4-dialkyl-2,4-dihydro-3H-1,2,4-triazole-3-thiones were prepared by the reaction of 1,4-dialkyl-5-phenylthio-1,2,4-triazolium salts with aqueous potassium carbonate or sodium sulfide in DMF, respectively.

A Study of the Behaviour of 2,4-Substituted Thiosemicarbazides toward Orthoesters: Formation of Mesoionic Compounds

The reactions beetwen 2,4-disubstituted thiosemicarbazides and orthoesters in refluxing xylene led to the formation of the 1,2,4-triazoline-5-thione ring and to the 1,2,4-triazolium-5-thiolate ring. The formation of the mesoionic componds is due to rearrangement of the easily available 2,4-disubstituted thiosemicarbazides to 1,4-disubstituted thiosemicarbazides under the reaction conditions adopted. This method can be usefully used for the synthesis of mesoionic compounds, especially in the case of the 2-methyl-4-phenylthiosemicarbazide.