1616779-78-2

Basic information

• Product Name: 6-(3,4-diaminophenoxy)-N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)hexanamide
• Synonyms: 6-(3,4-diaminophenoxy)-N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)hexanamide
• CAS NO: 1616779-78-2
• Molecular Weight: 360.413
• Mol File: 1616779-78-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-(3,4-diaminophenoxy)-N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)hexanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(3,4-diaminophenoxy)-N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)hexanamide(1616779-78-2)
• EPA Substance Registry System: 6-(3,4-diaminophenoxy)-N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)hexanamide(1616779-78-2)

Safety Data

• Hazardous Substances Data: 1616779-78-2(Hazardous Substances Data)

Upstream product

• 1616779-77-1 di-tert-butyl (4-((6-((2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)amino)-6-oxohexyl)oxy)-1,2-phenylene)dicarbamate 
• 1616779-76-0 6-(3,4-bis(tert-butoxycarbonylamino)phenoxy)hexanoic acid 
• 1616779-75-9 methyl 6-(3,4-bis(tert-butoxycarbonylamino)phenoxy)hexanoate 
• 14273-90-6 methyl 6-bromohexanoate 
• 14273-91-7 methyl 6-iodohexanoate 
• 1616779-74-8 di-tert-butyl (4-hydroxy-1,2-phenylene)dicarbamate 
• 615-72-5 3,4-diaminophenol 
• 610-81-1 4-hydroxy-2-nitroaniline 

Relevant articles and documents

A highly efficient oxidative condensation reaction for selective protein conjugation

We hereby report a mild and efficient coupling reaction between alkyl aldehydes and aryl diamines. In the presence of a Cu2+ or a Zn 2+ ion, oxygen (O2) in air is able to promote the oxidative condensation of the two readily preparable functional groups, forming stable benzimidazole linkages in neutral aqueous solution at room temperature (RT). We demonstrated that the reaction could be utilized to label a T4 lysozyme protein containing a chemically installed aryl diamine group with a fluorescent aldehyde dye molecule at 37 °C. the Partner Organisations 2014.