55854-42-7

Basic information

• Product Name: 2-Thiophenesulfonamide, 5-chloro-N-phenyl-
• CAS NO: 55854-42-7
• Molecular Formula: C10H8ClNO2S2
• Molecular Weight: 273.764
• Mol File: 55854-42-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Thiophenesulfonamide, 5-chloro-N-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Thiophenesulfonamide, 5-chloro-N-phenyl-(55854-42-7)
• EPA Substance Registry System: 2-Thiophenesulfonamide, 5-chloro-N-phenyl-(55854-42-7)

Safety Data

• Hazardous Substances Data: 55854-42-7(Hazardous Substances Data)

Upstream product

• 53595-66-7 2-chlorothiophene-5-sulfonamide 
• 108-94-1 cyclohexanone 
• 2766-74-7 5-chlorothien-2-ylsulfonyl chloride 
• 62-53-3 aniline 

Relevant articles and documents

Palladium-catalyzed arylation of aryl sulfonamides with cyclohexanones

Pd-catalyzed intermolecular aerobic dehydrogenative aromatizations have been developed for the arylation of aryl sulfonamides with cyclohexanones. Various N-aryl sulfonamides were selectively obtained in good yields using molecular oxygen as oxidant. The reaction tolerated a wide range of functionalities.

Nucleophilic Substitution at Sulphonyl Sulphur.Part 1. Reactivity of Tiophen-2-sulphonyl Halides in Water and Methanol-Acetonitrile

The reactions kinetics of substitued tiophen-2-sulphonyl chlorides and fluorides (5-OMe, 5-Me, H, 5-Cl, 4-NO2, 5-NO2) with anionic and neutral nucleophiles were studied in water at 25 deg C.For the reactions of chlorides with H2O,AcO-,and N3- and for the hydrolysis of fluorides U shaped Hammett plots were observed.For the reaction of sulphonyl chlorides with aniline,pyridine,imidazole,and OH- an approximately linear Hammett correlation is found.Common chloride ion effects on the hyrolysis rate constants appear to be absent.Nucleophilic substitution reactions of substitued thiophen-2-sulphonyl chlorides were also studied in MeOH-MeCN,where the Hammett equation is obeyed.The data appear consistent with an SN2-type mechanism wich can shift toward an SN1 or an SAN process depending on the nucleophile, on the ring substituent, and on the leaving group ability.The application of the More O'Ferrall and Thornton approaches for the prediction of substituent effects on the transition state structure seems to support the above interpretation.