6331-00-6

Usage

InChI:InChI=1/C9H12ClNO2S/c1-8-2-4-9(5-3-8)14(12,13)11-7-6-10/h2-5,11H,6-7H2,1H3

Upstream product

• 141-43-5 ethanolamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 14316-14-4 N-(2-hydroxy-ethyl)-4-methyl-benzenesulfonamide 
• 870-24-6 2-chloroethanamine hydrochloride 
• 3634-89-7 N-(p-toluenesulfonyl)aziridine 
• 91-22-5 quinoline 
• 541-41-3 chloroformic acid ethyl ester 
• 3981-23-5 N-(2-Iodethyl)-p-toluolsulfamid 
• 70-55-3 toluene-4-sulfonamide 
• 689-98-5 chloroethylamine 

Downstream Products

• 37075-71-1 N-(2-phenoxy-ethyl)-toluene-4-sulfonamide 
• 143699-27-8 N-(2-tosylaminoethyl)-1,3-propanediamine 
• 837-16-1 N-(2-isopropoxyethyl)-4-methylbenzenesulfonamide 
• 786-35-6 N-<2-tert.-Butyloxy-ethyl>-p-toluolsulfonamid 
• 786-37-8 N-<2-Isobutyloxy-ethyl>-p-toluolsulfamid 
• 791-60-6 N-Nitroso-N-<2-isobutyloxy-ethyl>-p-toluolsulfonamid 
• 3634-89-7 N-(p-toluenesulfonyl)aziridine 
• 834-65-1 N-(2-chloroethyl)-N-nitroso-p-toluenesulfonamide 
• 14316-16-6 N-tosylethylenediamine 
• 77429-97-1 N¹,N⁵-ditosyl-3-azapentane-1,5-diamine 
• 788-88-5 N-Nitroso-N-<2-isopropyloxy-ethyl>-p-toluolsulfonamid 
• 261912-63-4 N-(2-azidoethyl)-4-methylbenzenesulfonamide 

Relevant academic research and scientific papers

Complexes and Ligands

The present application provides ligands and fluorescent or luminescent complexes comprising these ligands.

Forthrightly monitoring ferroptosis induced by endoplasmic reticulum stresses through fluorescence lifetime imaging of microviscosity increases with a specific rotor

To test the hypothesis that the microviscosity changes of Endoplasmic Reticulum (ER) can be a useful indicator of ferroptosis promoted by ER Stresses (ERS), a new ER targeting viscosity rotor, L-Vis-1 was developed and applied in the quantitation of visco

Dual H-bond activation of NHC-Au(i)-Cl complexes with amide functionalized side-arms assisted by H-bond donor substrates or acid additives

Novel approach with amide-tethered H-bond donor NHC ligands enabled Au(i)-catalysis via H-bonding. The plain NHC-Au(i)-Cl complex catalysed conversions of terminal N-propynamides to oxazolines, and enyne cycloisomerization with an acid additive, in DCM at

Efficient N-acylation of sulfonamides using cesium salt of Wells–Dawson heteropolyacid as catalyst: Synthesis of new N-acyl sulfonamides and cyclic imides

N-acylation of substituted sulfonamides with different anhydrides in the presence of Cesium salt of Wells–Dawson heteropolyacid (Cs5HP2W18O62) as an efficient and reusable catalyst was investigated for the first time. ?Cs5HP2W18O62 was used with a catalytic amount in water as a green solvent. At room temperature, a series of N-acylsulfonamides were synthesized, while under refluxing conditions, new cyclic imides containing sulfonyl group were obtained. Atom-economy, high yields, easy work-up, as well as simple catalyst recovery and reusability are the key features of this procedure.

XANTHENE COMPOUND AND COLORING COMPOSITION

PROBLEM TO BE SOLVED: To provide a xanthene compound having good brightness and excellent fastness such as heat resistance, and a coloring composition thereof. SOLUTION: A xanthene compound is represented by the formula (1) (where, R1 and Rsup

Regioselective Synthesis of α- And γ-Amino Quinolinyl Phosphonamides Using N-Heterocyclic Phosphines (NHPs)

A regioselective phosphonylation of quinolines for the synthesis of α-amino quinolinyl phosphonamides and γ-amino quinolinyl phosphonamides has been developed under mild reaction conditions. An NHP-thiourea enables selective synthesis of α-amino quinolinyl phosphonamides by a Reissert-type reaction, and an NHP-tosylamide affords γ-amino quinolinyl phosphonamides via a 1,4-conjugate addition reaction. The corresponding amino quinolinyl phosphonate adducts were obtained in moderate to excellent yields (up to 99% yield) and regioselectivities (up to 99:1) with good functional group tolerance.

Synthesis and bioevaluation of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety

Two series of new 5-benzylidenethiazolidine-2,4-diones bearing benzenesulfonamide moiety were designed and synthesized. The synthesized compounds were evaluated for several biological activities, including cytotoxicity, histone deacetylation, and protein

LUMINESCENT MACROCYCLIC LANTHANIDE COMPLEXES

The present invention provides a novel class of macrocyclic compounds as well as complexes formed between a metal (e.g., lanthanide) ion and the compounds of the invention. Preferred complexes exhibit high stability as well as high quantum yields of lanthanide ion luminescence in aqueous media without the need for secondary activating agents. Preferred compounds incorporate hydroxy-isophthalamide moieties within their macrocyclic structure and are characterized by surprisingly low, non-specific binding to a variety of polypeptides such as antibodies and proteins as well as high kinetic stability. These characteristics distinguish them from known, open-structured ligands.

Zirconium tetrachloride mediated regioselective transformation of N-tosylaziridines into β-chlorosulfonamides

Regioselective ring opening of N-tosylaziridines has efficiently been carried out with ZrCl4 at room temperature to afford the corresponding β-chlorosulfonamides in high yields within a short reaction time.