2-Amino-5-methylthio-1,3,4-thiadiazole
ADVERTISEMENT
- Molecular formula
- C3H5N3S2
- CAS Number
- 2349-67-9
- IUPAC Name
- 5-methylsulfanyl-1,3,4-thiadiazol-2-amine
- Molecular Weight
- 148.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4700g/cm3
- Synonyms
- 5-(Methylsulfanyl)-1, 3, 4-thiadiazol-2-amine
Identification
Interesting facts
Interesting Facts about 5-methylsulfanyl-1,3,4-thiadiazol-2-amine
5-methylsulfanyl-1,3,4-thiadiazol-2-amine is a fascinating compound that belongs to the class of thiadiazoles, recognized for their diverse applications in the fields of chemistry and pharmacology. Here are some notable aspects to consider:
- Structure and Functionality: This compound features a unique ring structure that includes sulfur and nitrogen atoms, which contribute to its reactivity and potential applications. The substitution with a methylsulfanyl group enhances its chemical properties, making it an intriguing subject for research.
- Biological Significance: Compounds in the thiadiazole family are known for exhibiting biological activities. They are often studied for their antimicrobial, antifungal, and anticancer properties, which opens avenues for new drug development.
- Synthetic Pathways: The synthesis of 5-methylsulfanyl-1,3,4-thiadiazol-2-amine can be achieved via various methods that involve the reaction of thiocarbohydrazide with carbon disulfide and subsequent treatment with amines. This synthetic versatility adds to its appeal in chemical research.
- Potential Uses: Due to its potential as an agrochemical, this compound has drawn attention in crop protection studies. Researchers are exploring its efficacy against pests and pathogens that threaten agricultural yields.
- Research & Innovation: The compound is a subject of ongoing studies aimed at understanding its mechanism of action and exploring novel derivatives that might enhance its biological activity or improve selectivity.
As an intersection of chemistry, biology, and agriculture, 5-methylsulfanyl-1,3,4-thiadiazol-2-amine stands out as a compound that inspires further examination and innovation. It exemplifies how small molecular changes can lead to significant variations in activity and potential applications across multiple disciplines.