16078-86-7

Basic information

• Product Name: Phenol, 4-[(4-nitrophenyl)amino]-
• Synonyms: 4'-Hydroxy-4-nitrodiphenylamin;4-(4-Nitro-anilino)-phenol;N-(p-Nitrophenyl)-p-aminophenol;4'-Nitro-4-oxy-diphenylamin;4-Hydroxy-4'-nitrodiphenylamine;Phenol,4-(4-nitrophenyl)amino
• CAS NO: 16078-86-7
• Molecular Formula: C12H10N2O3
• Molecular Weight: 230.223
• Mol File: 16078-86-7.mol
• Article Data: 3

Chemical Properties

• Melting Point: 183 °C
• Boiling Point: 414.3±25.0 °C(Predicted)
• Density: 1.388±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Phenol, 4-[(4-nitrophenyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 4-[(4-nitrophenyl)amino]-(16078-86-7)
• EPA Substance Registry System: Phenol, 4-[(4-nitrophenyl)amino]-(16078-86-7)

Safety Data

• Hazardous Substances Data: 16078-86-7(Hazardous Substances Data)

Upstream product

• 623-11-0 1-methyl-4-nitrosobenzene 
• 858500-71-7 N-(4-hydroxy-phenyl)-N'-(4-nitro-benzenesulfonyl)-guanidine 
• 123-30-8 4-amino-phenol 
• 350-46-9 4-Fluoronitrobenzene 
• 7664-93-9 sulfuric acid 
• 540-38-5 p-Iodophenol 
• 100-01-6 4-nitro-aniline 
• 96-73-1 2-chloro-5-nitro-benzenesulfonic acid 

Downstream Products

• 6358-03-8 4-hydroxy-4'-aminodiphenylamine 
• 16124-67-7 (4-Allyloxy-phenyl)-(4-nitro-phenyl)-amine 
• 1375738-11-6 4-propoxy-4'-nitrodiphenylamine 
• 730-11-0 4-methoxy-N-(4-nitrophenyl)aniline 
• 1590-62-1 4-ethoxy-N-(4-nitrophenyl)aniline 
• 60457-51-4 4-butoxy-4'-nitrodiphenylamine 
• 1181377-25-2 4-benzyloxy-4'-nitrodiphenylamine 
• 101-64-4 Variamin Blau 
• 16124-59-7 4-Amino-4'-(2-diethylaminoethoxy)diphenylamine 
• 16124-65-5 [4-(4-Nitro-phenylamino)-phenoxy]-acetic acid ethyl ester 
• 60709-38-8 4-(2-Dimethylaminoethoxy)-4'-nitrodiphenylamine 
• 137445-04-6 (4-methoxy-methoxy-phenyl)-(4-nitro-phenyl)-amine 
• 832709-09-8 2-(1-hexyl-heptyl)-9-[4-(4-hydroxy-phenylamino)-phenyl]-anthra[2,1,9-def;6,5,10-d'e'f']diisoquinoline-1,3,8,10-tetraone 

Relevant articles and documents

Ligand-Enabled Gold-Catalyzed C(sp2)-N Cross-Coupling Reactions of Aryl Iodides with Amines

The first example of ancillary (P,N)-ligand-enabled gold-catalyzed C-N cross-coupling reactions of aryl iodides with amines is reported. The high generality of the reaction in de novo synthesis, late-stage modifications, and cascade processes to access functionalized indolinones and carbazoles underscores the synthetic potential of the presented strategy. Monitoring the reaction with ESI-HRMS and NMR provided strong evidence for the in situ formation of putative high valent Au(III) intermediates.

Hair dye compositions containing nitrodiphenylamine dyes and method for dyeing hair therewith

A hair dye composition comprising a fluid direct-dye hair dye vehicle suitable for application to human hair containing a tinctorially effective amount of a hair dye of formula: SPC1 In which: A. R is an electron donor functional group; B. y is a whole number from 0 to 1 inclusive; and C. x is a whole number from 1 to 2 inclusive. Also describes a method of dyeing hair using these compositions and further describes certain novel nitrodiphenylamine dyes.