5-Bromopyridine-3-sulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group attached to a brominated pyridine ring. It typically appears as a colorless to pale yellow liquid or solid, depending on its form and purity. This compound is known for its reactivity, particularly due to the presence of the sulfonyl chloride group, which can participate in nucleophilic substitution reactions. It is often used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The bromine atom in the pyridine ring can also serve as a site for further functionalization, making it a versatile intermediate in chemical synthesis. Additionally, 5-bromopyridine-3-sulfonyl chloride is sensitive to moisture and should be handled with care, as it can release hydrochloric acid upon hydrolysis. Proper safety precautions, including the use of personal protective equipment, are essential when working with this compound due to its corrosive nature and potential health hazards.

5-bromopyridine-3-sulfonyl chloride

65001-21-0: 3-Pyridinesulfonyl chloride, 5-bromo-, 5-Bromopyridine-3-sulphonyl Chloride, 65001-21-0

5-Bromopyridine-3-sulfonyl chloride

5-Bromopyridine-3-sulphonyl chloride

5-Bromopyridin-3-sulfonyl chloride is a recombinant protein that belongs to the group of arylsulphonamides. It can be used as an immunosuppressive drug in the treatment of respiratory diseases and has anti-inflammatory properties. 5-Bromopyridin-3-sulfonyl chloride is able to inhibit perforin, thereby inhibiting the release of inflammatory mediators. This protein also inhibits the production of cytokines, chemokines and prostaglandins. The pharmacokinetic properties of this protein are currently being studied in vivo models.

CAS 65001-21-0: 5-bromopyridine-3-sulfonyl chloride

5-Bromopyridine-3-sulfonyl chloride

Ref: 10-F067902

5-Bromopyridine-3-sulphonyl chloride

Ref: 54-OR9015

5-Bromopyridin-3-sulfonyl chloride

Ref: 3D-FB151170