561319-11-7

Basic information

• Product Name: Benzenesulfonamide, 4-methyl-N-[(3-methylphenyl)methylene]-
• CAS NO: 561319-11-7
• Molecular Formula: C15H15NO2S
• Molecular Weight: 273.356
• Mol File: 561319-11-7.mol
• Article Data: 23

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-methyl-N-[(3-methylphenyl)methylene]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-methyl-N-[(3-methylphenyl)methylene]-(561319-11-7)
• EPA Substance Registry System: Benzenesulfonamide, 4-methyl-N-[(3-methylphenyl)methylene]-(561319-11-7)

Safety Data

• Hazardous Substances Data: 561319-11-7(Hazardous Substances Data)

Upstream product

• 55962-05-5 [N-(p-tolylsulfonyl)imino]phenyliodinane 
• 620-23-5 m-tolyl aldehyde 
• 3262-39-3 1,2-bis(3-methylphenyl)ethylene 
• 4083-64-1 Tosyl isocyanate 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1160052-42-5 methyl 2-[(diphenylmethylene)amino]-3-(m-methylphenyl)-3-(p-toluenesulfonylamino)propanoate 
• 1393679-69-0 C₂₆H₂₈N₂O₂S 
• 1526980-20-0 (S,E)-4-methyl-N-(3-phenyl-1-(m-tolyl)allyl)benzenesulfonamide 
• 1619266-69-1 1,4-dimethyl 2-(o-tolyl(tosylimino)methyl)fumarate 
• 1619266-83-9 dimethyl 2-(m-tolyl)-1-tosyl-5-(trifluoromethyl)-1H-pyrrole-3,4-dicarboxylate 
• 1422237-58-8 N-((S)-((R)-3-bromo-2-oxoindolin-3-yl)(m-tolyl)methyl)-4-methylbenzenesulfonamide 
• 1132667-69-6 diethyl 3-(m-tolyl)-1-tosylaziridine-2,2-dicarboxylate 
• 1418179-16-4 C₂₆H₂₄N₂O₂S 
• 100-52-7 benzaldehyde 
• 1398511-94-8 N-((R)-((S)-3,4-dibromo-5-oxo-2,5-dihydrofuran-2-yl)(m-tolyl)methyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Facile synthesis, antimicrobial and antiviral evaluation of novel substituted phenyl 1,3-thiazolidin-4-one sulfonyl derivatives

A series of novel substituted phenyl 1, 3-thiazolidin-4-one sulfonyl derivatives 5 (a-t) were synthesized and screened for their in-vitro anti-microbial and anti-viral activity. The result of the anti-microbial assay demonstrated compounds 5d, 5f, 5g, 5h,

Enantioselective Aza-Reformatsky Reaction with Ketimines

Here, an enantioselective aza-Reformatsky reaction using acyclic ketimine substrates is presented. Using α-phosphorated ketimines as electrophilic substrates and a simple BINOL-derived ligand, phosphorated analogues of aspartic acid holding chiral tetrasubstituted carbons are efficiently obtained with excellent enantioselectivity through an asymmetric organocatalytic Reformatsky-type reaction. The phosphorated analogues of aspartic acid have been used for the synthesis of phosphorus-containing enantiopure tetrasubstituted β-lactams.

Formation of: N -sulfonyl imines from iminoiodinanes by iodine-promoted, N-centered radical sulfonamidation of aldehydes

A mild and operationally convenient formation of synthetically valuable N-sulfonyl imines from a range of aryl aldehydes by reaction with iminoiodinanes (PhINZ) and I2 has been developed. According to mechanistic experiments described within, the reaction is speculated to proceed through an unconventional light-promoted, N-centered radical (NCR) pathway involving a N,N-diiodosulfonamide reactive species. This method not only provides a new pathway toward the production of activated imines, but also serves as an example of a non-traditional means of carbonyl activation via an NCR species.