615565-35-0

Basic information

• Product Name: N,N'-(1,3-phenylenebis(methanylidene))bis(4-methylbenzenesulfonamide)
• Synonyms: N,N'-(1,3-phenylenebis(methanylidene))bis(4-methylbenzenesulfonamide)
• CAS NO: 615565-35-0
• Molecular Weight: 440.544
• Mol File: 615565-35-0.mol

Chemical Properties

• CAS DataBase Reference: N,N'-(1,3-phenylenebis(methanylidene))bis(4-methylbenzenesulfonamide)(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-(1,3-phenylenebis(methanylidene))bis(4-methylbenzenesulfonamide)(615565-35-0)
• EPA Substance Registry System: N,N'-(1,3-phenylenebis(methanylidene))bis(4-methylbenzenesulfonamide)(615565-35-0)

Safety Data

• Hazardous Substances Data: 615565-35-0(Hazardous Substances Data)

Upstream product

• 626-19-7 Isophthalaldehyde 
• 70-55-3 toluene-4-sulfonamide 

Downstream Products

• 1605282-17-4 (S,S)-N,N'-(1,3-phenylenebis((1H-indol-3-yl)methylene))bis(4-methylbenzenesulfonamide) 
• 1619919-70-8 N,N'-(1,3-phenylenebis(but-3-yne-1,1-diyl))bis(4-methylbenzenesulfonamide) 
• 1619919-74-2 N,N'-(1,3-phenylenebis(4-(3,4,5-trifluorophenyl)but-3-yne-1,1-diyl))bis(4-methylbenzenesulfonamide) 
• 1619919-72-0 N,N'-(1,3-phenylenebis(4-(3,5-bis(trifluoromethyl)phenyl)but-3-yne-1,1-diyl))bis(4-methylbenzenesulfonamide) 
• 1619919-84-4 1,3-bis(5-(4-(trifluoromethyl)phenyl)-1H-pyrrol-2-yl)benzene 
• 1619919-83-3 1,3-bis(5-(4-cyanophenyl)-1H-pyrrol-2-yl)benzene 
• 1619919-82-2 1,3-bis(5-(3,4,5-trifluorophenyl)-1H-pyrrol-2-yl)benzene 
• 1619919-80-0 1,3-bis(5-(3,5-bis(trifluoromethyl)phenyl)-1H-pyrrol-2-yl)benzene 

Relevant articles and documents

Arylpyrrole oligomers as tunable anion receptors

A novel type of arylpyrrole oligomer possessing an appropriate electropositive cavity has been designed, prepared and analysed for use as readily accessible receptors for negatively charged guests. Affinities of the receptors for various anions were determined by UV/Vis titration experiments and in depth insights into the host-guest interactions were gained by performing 1H NMR titration experiments and X-ray crystallographic structure analyses. Experimentally determined association constants were correlated with the calculated maximum electrostatic potentials of the electropositive cavities of the receptors, allowing estimation of the strengths of host-guest associations in similar compounds. The joint contribution of aryl C-H and pyrrole N-H hydrogens was shown to be key to a strong guest association, resulting in the arylpyrrole oligomers being efficient anion receptors. This journal is the Partner Organisations 2014.

Enantioselective continuous-flow production of 3-indolylmethanamines mediated by an immobilized phosphoric acid catalyst

A polystyrene-supported 1,1'-bi-2-naphthol derived phosphoric acid has been synthesized and applied in the enantioselective Friedel-Crafts reaction of indoles and sulfonylimines. The immobilized catalyst was highly active and selective, and gave rise to a