5-(2-Pyridyl)thiophene-2-sulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group attached to a thiophene ring, which is further substituted with a pyridine moiety. This compound typically appears as a solid or liquid, depending on the specific conditions, and is known for its reactivity due to the presence of the sulfonyl chloride group, which can participate in nucleophilic substitution reactions. It is often utilized in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The presence of both the thiophene and pyridine rings contributes to its unique electronic properties, making it useful in various applications, including pharmaceuticals and agrochemicals. Additionally, the compound may exhibit specific solubility characteristics in organic solvents, and its stability can be influenced by environmental factors such as moisture and temperature. Proper handling and storage are essential due to its reactive nature, particularly in the presence of nucleophiles.

5-(2-pyridyl)thiophene-2-sulfonyl chloride

151858-64-9: 5-(2-Pyridyl)thiophene-2-sulfonyl chloride is a chemical compound characterized by its sulfonyl chloride functional group attached to a thiophene ring, which is further substituted with a pyridine moiety. This compound typically appears as a solid or liquid, depending on the specific conditions, and is known for its reactivity due to the presence of the sulfonyl chloride group, which can participate in nucleophilic substitution reactions. It is often utilized in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The presence of both the thiophene and pyridine rings contributes to its unique electronic properties, making it useful in various applications, including pharmaceuticals and agrochemicals. Additionally, the compound may exhibit specific solubility characteristics in organic solvents, and its stability can be influenced by environmental factors such as moisture and temperature. Proper handling and storage are essential due to its reactive nature, particularly in the presence of nucleophiles.

CAS 151858-64-9

5-(2-pyridyl)thiophene-2-sulfonyl chloride

5-(Pyridin-2-yl)thiophene-2-sulphonyl chloride

Ref: 54-OR4077

5-Pyrid-2-ylthiophene-2-sulfonyl chloride

Ref: 10-F017373

5-(2-Pyridyl)thiophene-2-sulfonyl chloride

Ref: 3D-BGA85864