49633-28-5

Usage

Chemical class

Sulfonamide compounds

Structure

Symmetric bis-sulfonamide compound with two toluene-4-sulfonylamino functional groups attached to a benzene ring

Functionality

Provides functionality for reactions such as sulfonamide exchange, condensation, and polymerization

Applications

a. Building block for the synthesis of various organic compounds and materials
b. Pharmaceutical industry
c. Development of advanced materials and organic synthesis
d. Reagent in chemical reactions
e. Starting material for the synthesis of complex organic molecules

Upstream product

• 95-54-5 1,2-diamino-benzene 
• 98-59-9 p-toluenesulfonyl chloride 
• 3624-90-6 N-tosyl-1,2-diaminobenzene 
• 104-15-4 toluene-4-sulfonic acid 
• 98-57-7 4-chlorophenyl methyl sulfone 

Downstream Products

• 337959-14-5 1,7-bis-(toluene-4-sulfonyl)-2,3,4,5,6,7-hexahydro-1H-benzo[b][1,4]diazonine 
• 29627-62-1 N,N’-dimethyl-N,N’-di(p-toluenesulfonyl)-o-phenylenediamine 
• 64359-96-2 N¹,N²-diethyl-N¹,N²-ditosyl-o-phenylenediamine 
• 136269-09-5 N-allyl-N-(2-{allyl[(4-methylphenyl)sulfonyl]amino}phenyl)-4-methylbenzenesulfonamide 
• 205642-00-8 1-(N-methyl-N-4-toluenesulfonylamino)-2-(N-4-toluenesulfonylamino)benzene 
• 29543-34-8 1-[bis-(toluene-4-sulfonyl)-amino]-2-(toluene-4-sulfonylamino)-benzene 
• 70376-34-0 1,3-bis-(toluene-4-sulfonyl)-1,3-dihydro-benzo[1,2,5]thiadiazole 2-oxide 
• 29543-33-7 N,N'-Ditosyl-N-formyl-1,2-diaminobenzol 
• 27185-57-5 N,N'-(4-nitro-1,2-phenylene)bis(4-methylbenzenesulfonamide) 
• 78680-93-0 N,N'-(4-bromo-1,2-phenylene)bis(4-methylbenzenesulfonamide) 
• 91374-61-7 C₂₀H₁₈N₂O₅S₂ 
• 95-54-5 1,2-diamino-benzene 
• 101345-90-8 N,N'-ditosyl-1,2,3,5,6,7-hexahydro-4,1,7-benzoxadiazonine 
• 115368-19-9 C₂₂H₂₄N₂O₅S₂ 

Relevant academic research and scientific papers

Two-Dimensional Chemiresistive Covalent Organic Framework with High Intrinsic Conductivity

This paper describes the synthesis of a novel intrinsically conductive two-dimensional (2D) covalent organic framework (COF) through the aromatic annulation of 2,3,9,10,16,17,23,24-octa-aminophthalocyanine nickel(II) and pyrene-4,5,9,10-tetraone. The intr

A Stable and Conductive Metallophthalocyanine Framework for Electrocatalytic Carbon Dioxide Reduction in Water

Transformation of carbon dioxide to high value-added chemicals becomes a significant challenge for clean energy studies. Here a stable and conductive covalent organic framework was developed for electrocatalytic carbon dioxide reduction to carbon monoxide

Charge transport in phenazine-fused triphenylene discotic mesogens doped with CdS nanowires

Herein, we report the synthesis of oleylamine-capped CdS nanowires (NWs) and the dispersion of a small optimized amount of these NWs in the Colhphase of a recently synthesized phenazine-fused-triphenylene discotic liquid crystal (PFT DLC) to un

Nonradiative inter- and intramolecular energy transfer from the aromatic donor anisole to a synthesized photoswitchable acceptor system

We report steady state and time resolved fluorescence measurements on acetonitrile (ACN) solutions of the model compounds, energy donor anisole (A) and a photoswitchable acceptor N,N′-1,2-phenylene di-p-tosylamide (B) and the multichromophore (M) where A

Conductive Metallophthalocyanine Framework Films with High Carrier Mobility as Efficient Chemiresistors

The poor electrical conductivity of two-dimensional (2D) crystalline frameworks greatly limits their utilization in optoelectronics and sensor technology. Herein, we describe a conductive metallophthalocyanine-based NiPc-CoTAA framework with cobalt(II) te

Synthesis of spirocyclic aminosilanes with electron withdrawing substituents at nitrogen

The first synthesis of spirocyclic tetrasulfonamidosilanes is described. According to the X-Ray structure analysis of the most stable tetratosylamidosilane obtained the Silicon is bonded to four Nitrogen atoms in a spirocycle and surrounded by four Oxygen

A novel two-dimensional nickel phthalocyanine-based metal-organic framework for highly efficient water oxidation catalysis

Large π-conjugated conductive two-dimensional (2D) metal-organic frameworks (MOFs) via the bottom-up approach have recently emerged as novel and interesting 2D materials. For the first time, herein we demonstrate the design and successful bottom-up fabric

Ligand-Controlled Regiodivergence for Catalytic Stereoselective Semireduction of Allenamides

Ligand-controlled regiodivergence has been developed for catalytic semireduction of allenamides with excellent chemo- and stereocontrol. This system also provides an example of catalytic regiodivergent semireduction of allenes for the first time. The divergence of the semireduction is enabled by ligand switch with the same palladium pre-catalyst under operationally simple and mild conditions. Monodentate ligand XPhos exclusively promotes selective 1,2-semireduction to afford allylic amides, while bidentate ligand BINAP completely switched the regioselectivity to 2,3-semireduction, producing (E)-enamide derivatives.

Compound and preparation method thereof, and application of compound as n-type dopant

The invention provides a compound and a preparation method thereof, and application of the compound as an n-type dopant. The structural formula of the compound is shown as a formula (I) which is described in the specification. The compound can be used as

New cobalt(ii) coordination designs and the influence of varying chelate characters, ligand charges and incorporated group I metal ions on enzyme-like oxidative coupling activity

In transition-metal-mediated catalysis, designing new, well defined coordination architectures and subjecting them to catalysis testing under the same reaction conditions is a necessary tool for gaining an improved understanding of desirable active site geometries and characteristics. In this work, three ligands varying in chelation and charge characters (1= tridentate, dianionic N^N^N;2= bidentate, dianionic N^N;3= bidentate, neutral N^O) were synthesized and introduced as organic backbones around cobalt(ii) centres. Four multinuclear coordination assemblies incorporating various group I metal ions (i.e., (Na-Co1-i)2, (Na-Co1-e)2, (K-Co1-e)2and (Cs-Co1-e)2) and two mononuclear complexes (i.e.,Co2andCo3) were isolated, structurally characterized and studied as phenoxazinone synthase models. X-ray data and Continuous Shape Measure (CShM) calculations described unusual vacant trigonal bipyramidal geometries for (Na-Co1-i)2, (Na-Co1-e)2andCo3, trigonal bipyramids for (K-Co1-e)2and (Cs-Co1-e)2, and a tetrahedron forCo2. According to mass spectrometry data, the four multinuclear (MI-Co1-solvate)2complexes of ligand1easily dissociate in solution to yield the corresponding ions including a common mononuclearCo1unit. Testing as models in the oxidative coupling ofo-aminophenol revealed that an increasing chelate character of the organic ligand backbone produces an undesirable catalyst activity reduction. Furthermore, the similarity in coupling efficiencies observed among complexes (Na-Co1-i)2, (Na-Co1-e)2, (K-Co1-e)2and (Cs-Co1-e)2proves that the presence of varying group I metal ions contributed no catalytic effects to the coupling efficiencies and that theCo1species, which is generated by dissociation in solution, is the only active species responsible for the observed biomimetic behaviours. Therefore, the combination of anionic chelate ligands with easily detachable, neutral co-ligands (e.g., water or pyridine) around a cobalt(ii) centre could be recommended for the generation of a successful catalyst material, rather than the combination of a neutral chelate ligand with counter-anionic monodentate co-ligands like halides.