(4-Iodophenyl)methanesulfonyl chloride is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a phenyl ring that is further substituted with an iodine atom at the para position. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its reactivity, particularly in nucleophilic substitution reactions, where the sulfonyl chloride group can act as a leaving group. The presence of the iodine atom enhances its electrophilic character, making it useful in various synthetic applications, including the preparation of sulfonamides and other derivatives. Additionally, this compound is sensitive to moisture and should be handled with care, as it can hydrolyze to form the corresponding sulfonic acid. Safety precautions are essential when working with this substance due to its corrosive nature and potential health hazards associated with inhalation or skin contact. Overall, (4-iodophenyl)methanesulfonyl chloride is a valuable reagent in organic synthesis and medicinal chemistry.

(4-iodophenyl)methanesulfonyl chloride

345915-64-2: (4-Iodophenyl)methanesulfonyl chloride is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a phenyl ring that is further substituted with an iodine atom at the para position. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and form. It is known for its reactivity, particularly in nucleophilic substitution reactions, where the sulfonyl chloride group can act as a leaving group. The presence of the iodine atom enhances its electrophilic character, making it useful in various synthetic applications, including the preparation of sulfonamides and other derivatives. Additionally, this compound is sensitive to moisture and should be handled with care, as it can hydrolyze to form the corresponding sulfonic acid. Safety precautions are essential when working with this substance due to its corrosive nature and potential health hazards associated with inhalation or skin contact. Overall, (4-iodophenyl)methanesulfonyl chloride is a valuable reagent in organic synthesis and medicinal chemistry.

CAS 345915-64-2

(4-iodophenyl)methanesulfonyl chloride

(4-Iodophenyl)methanesulphonyl chloride

Ref: 54-OR60196

(4-Iodophenyl)methanesulfonyl chloride

Ref: 3D-VNA91564