56594-79-7

Usage

Chemical compound

Synthetic organic compound

Structure

Nitrophenyl group attached to the benzene ring

Usage

Production of hair dyes and cosmetic products

Color shades

Achieves shades of brown and black in hair dyes

Safety concerns

Associated with skin irritation and allergic reactions in some individuals

Environmental impact

Identified as a potential environmental pollutant

Disposal concerns

Raises questions about its use and disposal due to environmental impact

Upstream product

• 861546-60-3 2-(2-amino-anilino)-5-nitro-benzenesulfonic acid 
• 859786-88-2 N-(2-amino-phenyl)-N'-(4-nitro-benzenesulfonyl)-urea 
• 408511-07-9 N-(2-amino-phenyl)-N'-(4-nitro-benzenesulfonyl)-guanidine 
• 22492-14-4 1-(4-nitrophenyl)-1H-benzimidazole 
• 95-54-5 1,2-diamino-benzene 
• 586-78-7 para-nitrophenyl bromide 
• 612-36-2 2-nitro-N-(4-nitrophenyl)benzenamine 
• 7664-93-9 sulfuric acid 
• 51-17-2 benzoimidazole 
• 350-46-9 4-Fluoronitrobenzene 
• 39145-59-0 o-phenylenediamine hydrochloride 
• 615-28-1 o-phenylenediamine dihydrochloride 

Downstream Products

• 848393-58-8 1-(4-nitrophenyl)-1,3-dihydro-2H-benzo[d]imidazol-2-one 
• 86317-98-8 N-<2-(4-Nitrophenylamino)phenyl>benzamid 
• 78381-23-4 1-(4-aminophenyl)-1,2,3-benzotriazole 
• 86317-99-9 1-(4-nitrophenyl)-2-phenyl-1H-1,3-benzimidazole 

Relevant academic research and scientific papers

The Reaction of Some N-(Nitrophenyl)azoles with Alkali: Preparation of the Corresponding Azoxybenzenes. X-Ray Structure of 2,2'-Bis(1'',2'',4''-triazol-1''-yl)azoxybenzene

The reactions of some representative N-(nitrophenyl)azoles with boiling aqueous ethanolic potassium hydroxide solution gave the corresponding bis(azolyl)azoxybenzenes.It is deduced that, in these reactions, the N-attached azolyl groups concerned are acting as weak electron-withdrawing groups.The structure of 2,2'-bis(1'',2'',4''-triazol-1''-yl)azoxybenzene was determined in the solid state by X-ray crystallography.The monoclinic crystals belong to the space group P21/c with a 8.815(1), b 7.863(1), c 11.836(1) Angstroem, β 109.96(1) deg and Z 2.The structure was refined to an R index of 0.041 for 1172 observed terms.The midpoint of the exocyclic N=N bond lies on an inversion centre so that the azoxy oxygen is statistically distributed between two sites.The benzene ring atoms are coplanar to within experimental error, as are the triazole ring atoms, and the dihedral angle between the perpendiculars to the two rings is 35.3(3) deg.

SYNTHESES AND PROPERTIES OF SOME DERIVATIVES OF N--NAPHTHALIMIDE

Syntheses of N--naphthalimide and N--naphthalimide derivatives, unreported so far in the literature have been worked out, and the products are characterized.The usefulness of some of them as optical brightening agents has been established from their fluorescence spectra.The phenomenon of an intramolecular energy transfer from the benzotriazole to naphthalimide ring systems has been observed for the derivatives of N--naphthalimide.