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.
Synonyms
5-(Methylsulfanyl)-1,3,4-thiadiazol-2-amine
672-510-7
5319-77-7
2-Amino-5-(methylthio)-1,3,4-thiadiazole
5-(Methylthio)-1,3,4-thiadiazol-2-amine
1,3,4-Thiadiazol-2-amine, 5-(methylthio)-
5-methylsulfanyl-1,3,4-thiadiazol-2-amine
1,3,4-THIADIAZOLE, 2-AMINO-5-(METHYLTHIO)-
2-Amino-5-methylthio-1,3,4-thiadiazole
MFCD00175752
2-Amino-5-methylmercapto-1,3,4-thiadiazole
NSC-67524
NSC 67524
BRN 0118749
NSC67524
4-27-00-08165 (Beilstein Handbook Reference)
SCHEMBL750885
CHEMBL174202
DTXSID70201249
CHEBI:194593
4766G46MED
GEO-00174
STK722184
AKOS000112106
PS-4558
2-Amino-5-methylthio-1,3,4-thidiazole
5-methylthio-2-amino-1,3,4-thiadiazole
SY063539
1,4-Thiadiazol-2-amine, 5-(methylthio)-
2-Amino-5-methyl thio-1,3,4-thiadiazole
5-methylsulanyl-1,3,4-thiadiazol-2-amine
DB-004645
1,4-Thiadiazole, 2-amino-5-(methylthio)-
EN300-1263664
5-(Methylsulfanyl)-1,3,4-thiadiazol-2-amine #
2-Amino-5-(methylthio)-1,3,4-thiadiazole, 99%
Z18452635
F1386-0088
Solubility of 5-methylsulfanyl-1,3,4-thiadiazol-2-amine
The solubility of 5-methylsulfanyl-1,3,4-thiadiazol-2-amine can be influenced by several factors, including its molecular structure and environmental conditions. Here are key aspects to consider regarding its solubility:
In summary, understanding the solubility characteristics of 5-methylsulfanyl-1,3,4-thiadiazol-2-amine is not only key for its practical applications but also for further explorations in chemical synthesis and pharmacology. As the saying goes, “Like dissolves like,” and the interactions within the molecule will largely dictate its solubility behavior in various environments.