Interesting facts
Interesting Facts about 5-Chloro-3-phenyl-1,2,4-thiadiazole
5-Chloro-3-phenyl-1,2,4-thiadiazole is a fascinating compound that belongs to the class of thiadiazoles, which are characterized by their five-membered ring structures containing both sulfur and nitrogen atoms. This particular compound has piqued the interest of chemists for various reasons, including:
- Versatile Chemical Reactions: The presence of nitrogen and chlorine in its structure allows for a wide range of chemical transformations, making it a valuable intermediate for synthesizing more complex molecules.
- Biological Activity: Compounds similar to 5-chloro-3-phenyl-1,2,4-thiadiazole have been noted for their antimicrobial and herbicidal properties, highlighting its potential applications in pharmaceuticals and agriculture.
- Functionalized Derivatives: This compound serves as a key precursor for synthesizing various functionalized derivatives that exhibit enhanced properties, expanding its utility in research and industry.
- Research Interest: Due to its interesting structural attributes, it has become a subject of numerous studies aimed at discovering new properties and applications, driving forward the field of synthetic chemistry.
In the words of a chemist, “The exploration of thiadiazoles opens up pathways to innovation in drug development and materials science.” This quote underlines the significance of compounds like 5-chloro-3-phenyl-1,2,4-thiadiazole in advancing scientific knowledge and practical applications.
Overall, this compound serves as an exemplary model of how organic chemistry can lead to the discovery of substances with impactful real-world applications.
Synonyms
5-CHLORO-3-PHENYL-1,2,4-THIADIAZOLE
DTXSID80178953
RefChem:534737
DTXCID40101444
834-108-1
24255-23-0
5-Chloro-3-phenyl-[1,2,4]thiadiazole
1,2,4-Thiadiazole, 5-chloro-3-phenyl-
MFCD00096450
NSC518113
SCHEMBL930343
ZAA25523
SBB092073
AKOS004904277
AS-5184
NSC 518113
NSC-518113
1,4-Thiadiazole, 5-chloro-3-phenyl-
DA-20376
5-Chloro-3-phenyl-1,2,4-thiadiazole #
EN300-61279
Z963466992
Solubility of 5-chloro-3-phenyl-1,2,4-thiadiazole
The solubility of 5-chloro-3-phenyl-1,2,4-thiadiazole in various solvents is an intriguing aspect of this compound. Generally, the solubility behavior can be influenced by factors such as polarity, temperature, and the presence of functional groups. Below are some notable points regarding its solubility:
Furthermore, the interaction of the Cl atom and the phenyl group can lead to complex solubility behaviors, making this compound a subject of interest in various chemical applications. As a general guideline, it is advisable to perform solubility tests in different solvents to ascertain the best conditions for this compound.
In conclusion, while 5-chloro-3-phenyl-1,2,4-thiadiazole is not highly soluble in water, it finds better compatibility with certain organic solvents, which opens avenues for its use in practical applications. Always remember, “solubility is the key to unlocking the potential of your compound.”