98846-92-5

Basic information

• Product Name: tris[2-(N-tosylaminoethyl)]amine
• Synonyms: tris[2-(N-tosylaminoethyl)]amine
• CAS NO: 98846-92-5
• Molecular Weight: 608.804
• Mol File: 98846-92-5.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: tris[2-(N-tosylaminoethyl)]amine(CAS DataBase Reference)
• NIST Chemistry Reference: tris[2-(N-tosylaminoethyl)]amine(98846-92-5)
• EPA Substance Registry System: tris[2-(N-tosylaminoethyl)]amine(98846-92-5)

Safety Data

• Hazardous Substances Data: 98846-92-5(Hazardous Substances Data)

Upstream product

• 4097-89-6 2,2',2''-triaminotriethylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 3634-89-7 N-(p-toluenesulfonyl)aziridine 
• 6367-75-5 2-(tosylamino)ethyl p-toluenesulfonate 

Downstream Products

• 98846-93-6 N,N,N-tris<8-(tetrahydro-2H-pyran-2-yl)oxy-3-tosyl-6-oxa-3-azaoctyl>amine 
• 98846-96-9 N,N,N-tris<8-(tetrahydro-2H-pyran-2-yl)oxy-3-tosyl-3-azaoctyl>amine 
• 64819-96-1 4,10,16,22,27,33-hexatosyl-7,19,30-trioxa-1,4,10,13,16,22,27,33-octaazabicyclo<11.11.11>pentatriacontane 
• 98847-02-0 N,N,N-tris<12-(tetrahydro-2H-pyran-2-yl)oxy-3-tosyl-3-azadodecyl>amine 
• 165262-71-5 N,N,N-tris(((7-tetrahydro-2-pyranyl)oxy)-3-tosyl-3-azaheptyl)amine 
• 180618-50-2 3-[[2-(Bis-{2-[(2-methoxycarbonyl-ethyl)-(toluene-4-sulfonyl)-amino]-ethyl}-amino)-ethyl]-(toluene-4-sulfonyl)-amino]-propionic acid methyl ester 
• 750635-80-4 2,9-[2,5,8-triaza-2,8-ditosyl-5-(N-tosylaminoethy)]-[9]-1,10-phenanthrolinophane 
• 784209-73-0 C₃₆H₄₅N₇O₆S₃ 
• 914480-41-4 C₃₆H₅₇N₇O₆S₃ 
• 180618-51-3 N,N',N''-[nitrilo(ethane-2,1-diyl)]tris[N-(3-hydroxypropyl)-4-methylbenzenesulfonamide] 
• 98846-94-7 6,6',6''-tritosyl-8,8',8''-nitrilotri(3-oxa-6-azaoctanol) 
• 165262-72-6 N,N,N-tris(7-hydroxy-3-tosyl-3-azaheptyl)amine 

Relevant articles and documents

Manganese(ii) complexes of scorpiand-like azamacrocycles as MnSOD mimics

MnII complexes of scorpiand-type azamacrocycles constituted by a tretrazapyridinophane core appended with an ethylamino tail including 2- or 4-quinoline functionalities show very appealing in vitro SOD activity. The observed behaviour is relate

Flexible, N-sulfonyl-substituted aliphatic amine ligands in palladium-catalyzed Suzuki–Miyaura C–C coupling: Influence of substituents bulkiness and co-ligand size

Widespread use of commercially available palladium precatalysts is limited by high costs and their synthetic challenges. In this report, series of synthetically affordable, phosphine-free ligands were examined as supports for palladium active centers. 2-(

In vitro activity of scorpiand-like azamacrocycle derivatives in promastigotes and intracellular amastigotes of Leishmania infantum and Leishmania braziliensis

The activity of a family scorpiand-like azamacrocycles against Leishmania infantum and Leishmania braziliensis was studied using promastigotes, axenic and intracellular amastigotes forms. All the compounds are more active and less toxic than meglumine ant