4403-78-5

Basic information

• Product Name: N,N'-Bis(ethylene)-p-Toluenesulfonamide
• Synonyms: N,N''-ETHYLENEBIS-P-TOLUENESULFONAMIDE;N,N'-di-p-tosylethylenediamine;1,2-Bis(tosylamino)ethane;N,N'-Ditosyl-1,2-ethanediamine;N,N'-Ditosylethane-1,2-diamine;N,N'-Ditosylethylenediamine;N,N'-Ethylenebis(4-methylbenzenesulfonamide);4-methyl-N-[2-[(4-methylphenyl)sulfonylamino]ethyl]benzenesulfonamide
• CAS NO: 4403-78-5
• Molecular Formula: C₁₆H₂₀N₂O₄S₂
• Molecular Weight: 368.48
• Mol File: 4403-78-5.mol
• Article Data: 45

Chemical Properties

• Boiling Point: 549.934 °C at 760 mmHg
• Flash Point: 286.39 °C
• Appearance: /
• Density: 1.297 g/cm³
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N,N'-Bis(ethylene)-p-Toluenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-Bis(ethylene)-p-Toluenesulfonamide(4403-78-5)
• EPA Substance Registry System: N,N'-Bis(ethylene)-p-Toluenesulfonamide(4403-78-5)

Safety Data

• Hazardous Substances Data: 4403-78-5(Hazardous Substances Data)

Usage

Uses

N,N''-di-p-Tosylethylenediamine is a reactant in the synthesis of cyclohexane-1,2-bis(sulfonamide) .

Upstream product

• 107-15-3 ethylenediamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 1080-44-0 N-Tosylglycine 
• 74-89-5 methylamine 
• 49584-26-1 p-cyanobenzenesulfonyl chloride 
• 333-18-6 1,2-diaminoethane dihydrochloride 
• 613-91-2 acetophenone oxime 
• 64773-90-6 C₁₆H₁₈N₄O₆S₂ 
• 1821-99-4 N,N'-bis(trimethylsilyl)ethylenediamine 
• 14034-59-4 ethylenediamine p-toluenesulfonate 
• 98-88-4 benzoyl chloride 
• 70-55-3 toluene-4-sulfonamide 
• 106-93-4 ethylene dibromide 

Downstream Products

• 135524-84-4 Phenyl-[3-phenyl-1,4-bis-(toluene-4-sulfonyl)-piperazin-2-yl]-methanone 
• 103402-34-2 N,N'-didodecyl-N,N'-ethanediyl-bis-toluene-4-sulfonamide 
• 115368-12-2 N³,N⁶-ditosyl-3,6-diaza-1,8-octanediol 
• 115368-14-4 N-2-hydroxyethyl-N,N'-ditosylethylenediamine 
• 110663-50-8 4,7-ditoluenesulfonyl-1,4,7,10-tetraazacyclotridecane-2,9-dione 
• 122095-48-1 4,7-ditoluenesulfonyl-1,4,7,10-tetraazacyclotridecane-2,9-dione 
• 344425-32-7 N,N'-bis(p-toluenesulfonyl)ethylenediamido(1,5-cyclooctadiene)platinum(II) 
• 836637-10-6 2-bromo-1,3-ditosyl-1,3,2-diazaborolidine 
• 821785-00-6 2-chloro-1,3-bis(toluenesulfonyl)-1,3,2-diazaborolidine 
• 2758-80-7 ethyl N,N'-di-(p-toluenesulfonyl)piperazine-2-carboxylate 

Relevant articles and documents

1,2-Bis(N-fluoro-p-toluenesulfon-amido)ethane chloroform solvate

The title compound, N,N′-difluoro-N,N′-ethylenedi-p-toluenesulfonamide, C16H18F2N2O4S2 ·CHCl3, is a novel stable compound of the N-F class of reagents containing two R2/sub

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.

CHELATOR COMPOSITIONS FOR RADIOMETALS AND METHODS OF USING SAME

A chelator having the general structure (I) for chelating radiometals such as 225Ac under mild conditions is provided. (I) The chelator can be coupled to a biological targeting moiety to facilitate targeted delivery of the chelated radiometal i