104779-70-6

Basic information

• Product Name: 1,2,4,5-Benzenetetramine, N,N,N',N',N'',N'',N''',N'''-octamethyl-
• Synonyms: 1,2,4,5-Benzenetetramine,N,N,N',N',N'',N'',N''',N'''-octamethyl
• CAS NO: 104779-70-6
• Molecular Formula: C14H26N4
• Molecular Weight: 250.38300
• Mol File: 104779-70-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 377.2±42.0 °C(Predicted)
• Density: 1.037±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,2,4,5-Benzenetetramine, N,N,N',N',N'',N'',N''',N'''-octamethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4,5-Benzenetetramine, N,N,N',N',N'',N'',N''',N'''-octamethyl-(104779-70-6)
• EPA Substance Registry System: 1,2,4,5-Benzenetetramine, N,N,N',N',N'',N'',N''',N'''-octamethyl-(104779-70-6)

Safety Data

• Hazardous Substances Data: 104779-70-6(Hazardous Substances Data)

Usage

Uses

1,2,4,5-Tetrakis(dimethylamino)benzene is an electron donor with unusual properties.

Upstream product

• 881890-22-8 3,6-difluoro-1,2,4,5-tetrakis(dimethylamino)benzene 
• 50-00-0 formaldehyd 
• 4506-66-5 1,2,4,5-benzenetetraamine tetrahydrochloride 

Downstream Products

• 104779-73-9 N,N,N',N',N'',N'',N''',N'''-Octamethyl-benzene-1,2,4,5-tetraamine; compound with 2-(4-dicyanomethylene-cyclohexa-2,5-dienylidene)-malononitrile 
• 108794-72-5 1,2,4,5-tetrakis(dimethylamino)benzene dihydrobromide 

Relevant articles and documents

On the causes of potential inversion in 1,2,4,5-tetrakis(amino)benzenes

(Graph Presented) Three 3,6-difluoro-1,2,4,5-tetrakis(amino)benzene compounds, bearing dimethylamino (1), piperidin-1-yl (3), or morpholin-1-yl (5) substituents, have been synthesized and subsequently defluorinated to give the corresponding 1,2,4,5-tetrak

New 'proton sponges', 13[≠] syntheses, structures and basicities of 1,2,4,5-tetrakis(dimethylamino)benzene and 2,3,6,7- tetrakis(dimethylamino)naphthalene

1,2,4,5-Tetrakis(dimethylamino)benzene (4) and 2,3,6,7- tetrakis(dimethylamino)naphthalene (5) were prepared and structurally determined. Electron-donor functions, protonation, and the geometry of intramolecular hydrogen bonds are discussed. By oxidation of 4 to its dication the benzenoid aromaticity is cancelled in favour of two independent cyanine-type units as determined by X-ray structure analysis.

1,2,4,5-Tetrakis(dimethylamino)benzol, ein neuer Elektron-Donor mit ungewoehnlichen Eigenschaften

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