2-Chloro-5-(trifluoromethyl)-1,3,4-thiadiazole is a heterocyclic compound characterized by the presence of a thiadiazole ring, which consists of two nitrogen atoms and one sulfur atom within a five-membered ring. The compound features a chlorine atom at the 2-position and a trifluoromethyl group (-CF3) at the 5-position, contributing to its unique chemical properties. This structure imparts significant polarity and potential reactivity, making it useful in various applications, including agrochemicals and pharmaceuticals. The trifluoromethyl group enhances lipophilicity and metabolic stability, while the chlorine atom can participate in nucleophilic substitution reactions. The compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions, although it should be handled with care due to the presence of halogenated and sulfur-containing functionalities. Its synthesis often involves the reaction of appropriate precursors under controlled conditions, and it may be analyzed using techniques such as NMR, IR spectroscopy, and mass spectrometry to confirm its structure and purity.

2-chloro-5-(trifluoromethyl)-1,3,4-thiadiazole

53645-98-0: 2-Chloro-5-(trifluoromethyl)-1,3,4-thiadiazole is a heterocyclic compound characterized by the presence of a thiadiazole ring, which consists of two nitrogen atoms and one sulfur atom within a five-membered ring. The compound features a chlorine atom at the 2-position and a trifluoromethyl group (-CF3) at the 5-position, contributing to its unique chemical properties. This structure imparts significant polarity and potential reactivity, making it useful in various applications, including agrochemicals and pharmaceuticals. The trifluoromethyl group enhances lipophilicity and metabolic stability, while the chlorine atom can participate in nucleophilic substitution reactions. The compound is typically a solid at room temperature and may exhibit moderate to high stability under standard conditions, although it should be handled with care due to the presence of halogenated and sulfur-containing functionalities. Its synthesis often involves the reaction of appropriate precursors under controlled conditions, and it may be analyzed using techniques such as NMR, IR spectroscopy, and mass spectrometry to confirm its structure and purity.

2-Chloro-5-(trifluoromethyl)-1,3,4-thiadiazole

CAS 53645-98-0

2-chloro-5-(trifluoromethyl)-1,3,4-thiadiazole

2-Chloro-5-(trifluoromethyl)-1,3,4-thiadiazole

Ref: 54-PC401017

2-Chloro-5-trifluoromethyl-1,3,4-thiadiazole

Ref: 10-F045205