2-Phenyl-1,3-thiazole-4-carbonyl chloride 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 phenyl group attached to the thiazole ring contributes to its aromatic properties, while the carbonyl chloride functional group indicates that it is an acyl chloride, making it reactive and useful in various chemical reactions, particularly in acylation processes. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity is primarily due to the carbonyl chloride group, which can readily participate in nucleophilic substitution reactions. Additionally, 2-phenyl-1,3-thiazole-4-carbonyl chloride may have applications in the synthesis of pharmaceuticals, agrochemicals, or other fine chemicals, owing to its ability to serve as an intermediate in the formation of more complex molecules. Safety precautions should be taken when handling this compound, as acyl chlorides can be corrosive and may release harmful gases upon reaction with water or moisture.

2-phenyl-1,3-thiazole-4-carbonyl chloride

36094-04-9: 2-Phenyl-1,3-thiazole-4-carbonyl chloride 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 phenyl group attached to the thiazole ring contributes to its aromatic properties, while the carbonyl chloride functional group indicates that it is an acyl chloride, making it reactive and useful in various chemical reactions, particularly in acylation processes. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity is primarily due to the carbonyl chloride group, which can readily participate in nucleophilic substitution reactions. Additionally, 2-phenyl-1,3-thiazole-4-carbonyl chloride may have applications in the synthesis of pharmaceuticals, agrochemicals, or other fine chemicals, owing to its ability to serve as an intermediate in the formation of more complex molecules. Safety precautions should be taken when handling this compound, as acyl chlorides can be corrosive and may release harmful gases upon reaction with water or moisture.

4-Thiazolecarbonylchloride, 2-phenyl-

2-Phenyl-1,3-thiazole-4-carbonyl chloride

CAS 36094-04-9

2-phenyl-1,3-thiazole-4-carbonyl chloride

4-Thiazolecarbonylchloride, 2-phenyl-

Ref: IN-DA007BE9

2-Phenyl-1,3-thiazole-4-carbonyl chloride

Ref: 54-OR23283