83626-78-2

Basic information

• Product Name: 2-{6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl}-isoindole-1,3-dione
• Synonyms: 2-{6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl}-isoindole-1,3-dione;2-(6-((6-(1-Oxoisoindolin-2-yl)hexyl)disulfanyl)hexyl)isoindoline-1,3-dione
• CAS NO: 83626-78-2
• Molecular Formula: C28H34N2O3S2
• Molecular Weight: 510.71116
• Mol File: 83626-78-2.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-{6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl}-isoindole-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-{6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl}-isoindole-1,3-dione(83626-78-2)
• EPA Substance Registry System: 2-{6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl}-isoindole-1,3-dione(83626-78-2)

Safety Data

• Hazardous Substances Data: 83626-78-2(Hazardous Substances Data)

Usage

Chemical compound

2-6-[6-(1-Oxo-1,3-dihydro-isoindol-2-yl)-hexyldisulfanyl]-hexyl-isoindole-1,3-dione

Class

Isoindole-1,3-dione derivative

Structure

Central isoindole-1,3-dione ring with two side chains

Side chains

Hexyldisulfanyl group
1-oxo-1,3-dihydro-isoindol-2-yl group

Potential applications

Pharmaceuticals and organic synthesis

Unique structure

May exhibit interesting biological activities

Uses

Building block for synthesis of complex molecules

Further research

Needed for full understanding of properties and uses.

Upstream product

• 24566-79-8 2-(6-bromohexyl)isoindole-1,3-dione 
• 629-03-8 1 ,6-dibromohexane 
• 1074-82-4 potassium phtalimide 

Downstream Products

• 83626-66-8 N-(4-{6-[6-(4-Acetylamino-benzenesulfonylamino)-hexyldisulfanyl]-hexylsulfamoyl}-phenyl)-acetamide 
• 118077-46-6 6,6'-disulfanediylbis(hexan-1-amine) dihydrochloride 

Relevant articles and documents

New organic picolylamine-type ligands and electrochemical study of their complexation with Cu(MeCN)4ClO4

A series of novel organic ligands with dipicolylamine and disulfide groups connected by polymethylene, alkylaryl, alkoxyaryl, or alkoxycarbonyl linker was synthesized. The electrochemical study by cyclic voltammetry was carried out for two synthesized lig

Synthesis of ω-(4-aminophenylsulfonamido)alkyl disulfides and thiosulfates and their activity against dihydropteroate synthetase from sulfanilamide-resistant Neisseria gonorrhoeae

A series of ω-(4-aminophenylsulfonamido)alkyl disulfides and ω-(4-aminophenylsulfonamido)alkanethiosulfates was synthesized from the reaction of p-acetamidobenzenesulfanilyl chloride and either the aminoalkyl disulfide dihydrobromide or the aminoalkyl bro