2-Chloro-4-phenylthiazole is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of a chlorine atom at the second position and a phenyl group at the fourth position of the thiazole ring contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It may exhibit antimicrobial, antifungal, or herbicidal properties, making it of interest in various fields of research. The molecular structure allows for specific interactions with biological targets, which can be explored for therapeutic purposes. Additionally, 2-Chloro-4-phenylthiazole is soluble in organic solvents, and its reactivity can be influenced by the presence of the chlorine substituent, which can participate in nucleophilic substitution reactions. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

2-Chloro-4-phenylthiazole

1826-23-9: 2-Chloro-4-phenylthiazole is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing both sulfur and nitrogen atoms. The presence of a chlorine atom at the second position and a phenyl group at the fourth position of the thiazole ring contributes to its unique chemical properties. This compound typically appears as a solid and is known for its potential applications in pharmaceuticals and agrochemicals due to its biological activity. It may exhibit antimicrobial, antifungal, or herbicidal properties, making it of interest in various fields of research. The molecular structure allows for specific interactions with biological targets, which can be explored for therapeutic purposes. Additionally, 2-Chloro-4-phenylthiazole is soluble in organic solvents, and its reactivity can be influenced by the presence of the chlorine substituent, which can participate in nucleophilic substitution reactions. Safety data should be consulted for handling and usage, as with any chemical substance, to ensure proper precautions are taken.

CAS 1826-23-9

2-Chloro-4-phenylthiazole

Thiazole, 2-chloro-4-phenyl-

Ref: IN-DA0023ZV

2-Chloro-4-phenyl-1,3-thiazole

Ref: 54-OR1037785

2-Chloro-4-phenylthiazole

Ref: 10-F024114