4-(2-Methyl-1,3-thiazol-4-yl)benzenesulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. The presence of the thiazole ring contributes to its heterocyclic nature, providing unique electronic properties and potential biological activity. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as dichloromethane and acetone, but is generally insoluble in water due to its hydrophobic characteristics. It is often used as a reagent in the synthesis of sulfonamides and other sulfonyl-containing compounds, making it valuable in pharmaceutical and agrochemical research. The sulfonyl chloride group is particularly reactive, allowing for the introduction of various nucleophiles, which can lead to the formation of diverse chemical entities. As with many sulfonyl chlorides, it should be handled with care due to its potential to release hydrochloric acid upon hydrolysis and its irritant properties.

4-(2-methyl-1,3-thiazol-4-yl)benzenesulfonyl chloride

852180-73-5: 4-(2-Methyl-1,3-thiazol-4-yl)benzenesulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. The presence of the thiazole ring contributes to its heterocyclic nature, providing unique electronic properties and potential biological activity. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as dichloromethane and acetone, but is generally insoluble in water due to its hydrophobic characteristics. It is often used as a reagent in the synthesis of sulfonamides and other sulfonyl-containing compounds, making it valuable in pharmaceutical and agrochemical research. The sulfonyl chloride group is particularly reactive, allowing for the introduction of various nucleophiles, which can lead to the formation of diverse chemical entities. As with many sulfonyl chlorides, it should be handled with care due to its potential to release hydrochloric acid upon hydrolysis and its irritant properties.

CAS 852180-73-5

4-(2-methyl-1,3-thiazol-4-yl)benzenesulfonyl chloride

4-(2-Methyl-1,3-thiazol-4-yl)benzenesulfonyl chloride

Ref: IN-DA004Q99

4-(2-Methyl-1,3-thiazol-4-yl)benzenesulphonyl chloride

Ref: 54-OR4395

4-(2-Methyl-thiazol-4-yl)-benzenesulfonyl chloride

Ref: 10-F047463