4284-51-9

Basic information

• Product Name: Methanesulfonamide, N-(4-chlorophenyl)-
• CAS NO: 4284-51-9
• Molecular Formula: C7H8ClNO2S
• Molecular Weight: 205.665
• Mol File: 4284-51-9.mol
• Article Data: 27

Chemical Properties

• CAS DataBase Reference: Methanesulfonamide, N-(4-chlorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanesulfonamide, N-(4-chlorophenyl)-(4284-51-9)
• EPA Substance Registry System: Methanesulfonamide, N-(4-chlorophenyl)-(4284-51-9)

Safety Data

• Hazardous Substances Data: 4284-51-9(Hazardous Substances Data)

Upstream product

• 106-47-8 4-chloro-aniline 
• 7143-01-3 Methanesulfonic anhydride 
• 1197-22-4 N-phenylmethanesulfonamide 
• 380430-57-9 4-(methylsulfonylamino)phenyl boronic acid 
• 637-87-6 1-Chloro-4-iodobenzene 
• 3144-09-0 methanesulfonamide 
• 1679-18-1 4-Chlorophenylboronic acid 
• 624-90-8 Methanesulfonyl azide 
• 106-39-8 bromochlorobenzene 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 1894-97-9 N-(4-Chloro-phenyl)-N-(dichloro-fluoro-methylsulfanyl)-methanesulfonamide 
• 612-57-7 6-chloroquinoline 
• 333383-75-8 N-(4-chloro-phenyl)-N-(3-oxo-propyl)-methanesulfonamide 
• 149944-34-3 N-(4-chlorophenyl)-2-hydroxyethanesulfonamide 
• 71270-67-2 N-2-oxopropyl-4'-chloro-methanesulphonanilide 
• 71273-57-9 2-[(4-Chloro-phenyl)-methanesulfonyl-amino]-N,N-diethyl-acetamide 
• 71273-56-8 N-(4-Chloro-phenyl)-N-cyanomethyl-methanesulfonamide 
• 22729-74-4 N-(4-Chloro-phenyl)-N-(1,1,2,2-tetrachloro-2-fluoro-ethylsulfanyl)-methanesulfonamide 
• 16241-65-9 N-(Trichlormethyl-dithio)-methansulfonsaeure-(p-chlor-anilid) 
• 66235-99-2 N-allyl-N-(4-chloro-phenyl)-methanesulfonamide 

Relevant articles and documents

Meta Selective C-H Borylation of Sterically Biased and Unbiased Substrates Directed by Electrostatic Interaction

An electrostatically directed meta borylation of sterically biased and unbiased substrates is described. The borylation follows an electrostatic interaction between the partially positive and negative charges between the ligand and substrate. With this strategy, it has been demonstrated that a wide number of challenging substrates, especially 4-substituted substrates, can selectively be borylated at the meta position. Moreover, unsubstituted substrates also displayed excellent meta selectivity. The reaction employs a bench-stable ligand and proceeds at a milder temperature, precluding the need to synthesize a bulky and sophisticated ligand/template.

Aniline compound for preventing and treating mental disorder diseases

The invention discloses an aniline compound for preventing and treating mental disorder diseases, wherein the structure of the compound is represented by a formula I, and each substituent is defined in the specification and claims. The invention also disc

Facile Chan-Lam coupling using ferrocene tethered N-heterocyclic carbene-copper complex anchored on graphene

Ferrocene tethered N-heterocyclic carbene-copper complex anchored on graphene ([GrFemImi]NHC@Cu complex) has been synthesized by covalent grafting of ferrocenyl ionic liquid in the matrix of graphene followed by metallation with copper (I) iodide. The [GrFemImi]NHC@Cu complex has been characterized by fourier transform infrared (FT-IR), fourier transform Raman (FT-Raman), CP-MAS 13C NMR spectroscopy, transmission electron microscopy (TEM), thermogravimetric analysis (TGA), energy dispersive X-ray (EDX) analysis, X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) surface area analysis and X-ray diffractometer (XRD) analysis. This novel complex served as a robust heterogeneous catalyst for the synthesis of bioactive N-aryl sulfonamides from variety of aryl boronic acids and sulfonyl azides in ethanol by Chan-Lam coupling. Recyclability experiments were executed successfully for six consecutive runs.