71006-78-5

Usage

Imidazole derivative

It is a derivative of the imidazole group The compound has a structure based on the imidazole ring, which is a key structural component in many biologically active molecules.

Nitro group presence

Contains a nitro group (-NO2) The presence of this functional group can influence the reactivity and properties of the compound.

Physical state

Colorless to pale yellow liquid The compound is in a liquid state at room temperature, with a color ranging from colorless to pale yellow.

Molecular weight

220.20 g/mol The mass of one mole of the compound is 220.20 grams.

Pharmaceutical applications

Potential use in anti-microbial and anti-fungal agents The compound may be effective in fighting against microbial and fungal infections, making it a valuable candidate for pharmaceutical development.

Upstream product

• 4150-51-0 6,7-dihydro-2,11-dimethyldipyrido<1,2-a:2',1'-c>pyrazinediium dibromide 
• 73852-95-6 6,7,8,9-tetrahydro-2,13-dimethyldipyrido<1,2-a:2',1'-c><1,4>diazocinediium dibromide 
• 94887-37-3 6,7-dihydro-2,3,10,11-tetramethyldipyrido<1,2-a:2'.1'-c>pyrazinediium dibromide 
• 94887-38-4 7,8-dihydro-2,3,11,12-tetramethyl-6H-dipyrido<1,2-a:2',1'-c><1,4>diazepinediium dibromide 
• 5875-57-0 7,8-dihydro-2,12-dimethyl-6H-dipyrido<1,2-a:2',1'-c><1,4>diazepinediium dibromide 

Relevant academic research and scientific papers

Radical Cations of some Low-potential Viologen Compounds; Reduction Potentials and Electron-transfer Reactions

The one-electron reduction potentials (E1) of certain pyrazinediium, diazepinediium and diazocinediium viologen compounds substituted with methyl groups, V(2+), have been determined from the position of the one-electron transfer equilibria with reference compounds using pulse radiolysis.E1 ranges from -491 +/- 6 mV (vs NHE) for 6,7-dihydro-2,11-dimethyldipyridopyrazinediium dibromide (V21(2+)) to -832 +/- 11 mV for 6,7,8,9-tetrahydro-2,3,12,13-tetramethyldipyridodiazocinediium dibromide (V42(2+)).The rates of reduction by e(1-)aq were found to be independent of E1 whereas the rates of electron transfer from CO2(1-). and (CH3)2C.OH species do show a dependence on E1 for V(2+) compounds of lowest E1.Marcus-type treatment of the rate-constant data yields a rate constant of electron exchange between propan-2-oxyl radicals and acetone in the range (2-6)E6 dm3mol-1s-1 and between the radical cation of 6,7-dihydro-2,3,10,11-tetramethyldipyridopyrazinediium dibromide (V22.(1+)) and its unreduced form (V22(2+)) of 5E7 dm3mol-1s-1.