5-Chloro-1,2,3-thiadiazole is a heterocyclic compound characterized by a five-membered ring containing two nitrogen atoms, one sulfur atom, and one chlorine substituent. This compound is typically a colorless to pale yellow solid at room temperature and is known for its aromatic properties due to the presence of the thiadiazole ring. It exhibits moderate solubility in polar organic solvents, which can facilitate its use in various chemical reactions. The chlorine atom at the 5-position enhances its reactivity, making it a useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, 5-chloro-1,2,3-thiadiazole can participate in nucleophilic substitution reactions and is known for its potential biological activity, including antimicrobial and antifungal properties. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and reactivity make it a valuable compound in organic synthesis and medicinal chemistry.

5-Chloro-1,2,3-thiadiazole

4113-57-9: 5-Chloro-1,2,3-thiadiazole is a heterocyclic compound characterized by a five-membered ring containing two nitrogen atoms, one sulfur atom, and one chlorine substituent. This compound is typically a colorless to pale yellow solid at room temperature and is known for its aromatic properties due to the presence of the thiadiazole ring. It exhibits moderate solubility in polar organic solvents, which can facilitate its use in various chemical reactions. The chlorine atom at the 5-position enhances its reactivity, making it a useful intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, 5-chloro-1,2,3-thiadiazole can participate in nucleophilic substitution reactions and is known for its potential biological activity, including antimicrobial and antifungal properties. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and reactivity make it a valuable compound in organic synthesis and medicinal chemistry.

CAS 4113-57-9

5-Chloro-1,2,3-thiadiazole

5-Chloro-1,2,3-thiadiazole

Ref: IN-DA00BXYA

5-Chloro-1,2,3-thiadiazole

Ref: 10-F718559