115802-63-6

Basic information

• Product Name: N-(2-bromophenyl)-N-methyl-p-toluenesulfonamide
• Synonyms: N-(2-bromophenyl)-N-methyl-p-toluenesulfonamide
• CAS NO: 115802-63-6
• Molecular Weight: 254.126
• Mol File: 115802-63-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-(2-bromophenyl)-N-methyl-p-toluenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-bromophenyl)-N-methyl-p-toluenesulfonamide(115802-63-6)
• EPA Substance Registry System: N-(2-bromophenyl)-N-methyl-p-toluenesulfonamide(115802-63-6)

Safety Data

• Hazardous Substances Data: 115802-63-6(Hazardous Substances Data)

Upstream product

• 614-76-6 N-acetyl-2-bromoaniline 
• 106-95-6 allyl bromide 
• 615-36-1 2-bromoaniline 
• 107-18-6 allyl alcohol 
• 107-05-1 3-chloroprop-1-ene 
• 591-87-7 Allyl acetate 

Downstream Products

• 31676-46-7 1-(3-methylindolin-1-yl)ethanone 
• 4375-15-9 3-methyl-2,3-dihydro-1H-indole 

Relevant articles and documents

A Next-Generation Air-Stable Palladium(I) Dimer Enables Olefin Migration and Selective C?C Coupling in Air

We report a new air-stable PdI dimer, [Pd(μ-I)(PCy2tBu)]2, which triggers E-selective olefin migration to enamides and styrene derivatives in the presence of multiple functional groups and with complete tolerance of air. The same dimer also triggers extremely rapid C?C coupling (alkylation and arylation) at room temperature in a modular and triply selective fashion of aromatic C?Br, C?OTf/OFs, and C?Cl bonds in poly(pseudo)halogenated arenes, displaying superior activity over previous PdI dimer generations for substrates that bear substituents ortho to C?OTf.

Visible-light-induced photocatalytic reductive transformations of organohalides

A photo opportunity: A visible-light-excited iridium catalyst delivers electrons from an amine to an organohalide. The electron transfer then induces reductive scission of the carbon-halogen bond, generating the corresponding alkyl, alkenyl, and aryl radical that can undergo cyclization and hydrodehalogenation reactions. Copyright

THE REACTIONS OF ALLYL o-BROMOARYL ETHERS, N-ALLYL o-BROMOACETANILIDE, AND RELATED COMPOUNDS WITH TRIBUTYLTIN HYDRIDE IN THE PRESENCE OF ACTIVATED OLEFINS

o-Bromophenyl allyl ether, N-allyl o-bromoacetanilide, and related compounds reacted with tributyltin hydride in the presence of activated olefins to give 2,3-dihydrobenzofuran, 2,3-dihydroindole, and analogous derivatives in modest yields respectively vi