41071-23-2

Basic information

• Product Name: Phenoxy, 4-nitro-
• CAS NO: 41071-23-2
• Molecular Formula: C6H4NO3
• Molecular Weight: 138.103
• Mol File: 41071-23-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Phenoxy, 4-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenoxy, 4-nitro-(41071-23-2)
• EPA Substance Registry System: Phenoxy, 4-nitro-(41071-23-2)

Safety Data

• Hazardous Substances Data: 41071-23-2(Hazardous Substances Data)

Upstream product

• 4281-46-3 2-hydroxypropyl-p-nitrophenyl phosphate 
• 100-00-5 4-chlorobenzonitrile 
• 100-02-7 4-nitro-phenol 
• 603-76-9 C₉H₉N⁽¹⁺⁾ 
• 14609-74-6 p-nitrophenolate 
• 505-14-6 (SCN)2 anion radical 

Downstream Products

• 14609-74-6 p-nitrophenolate 
• 603-76-9 C₉H₉N⁽¹⁺⁾ 

Relevant articles and documents

Solid state generation of phenoxyl radicals through β-fragmentation from specifically designed diazenes. An ESR investigation

Upon irradiation at room temperature, symmetrical diazene precursors enabled the formation of phenoxyl radicals through β-fragmentation reaction in the solid state. This traceless generation of phenoxyl radicals was investigated by ESR. This study showed that although the fragmentation of β-phenoxy radicals is a slow process in solution, it could be useful in solid state thanks to the absence of faster competitive pathways.

Localized electron transfer in nonpoiar solution: reaction of phenols and thiophenols with free solvent radical cations

Free electron transfer (FET) is understood as the reaction of free and uncorrelated solvent parent radical cations with solutes characterized by a lower ionization potential than those of the solvent. We studied electron transfer from phenols and thiophen

The one-electron reduction potential of 4-substituted phenoxyl radicals in water

By means of pulse radiolysis the one-electron reduction potentials of twelve 4-substituted phenoxy radicals have been determined. The main reference used was the ClO2./ClO2- couple. By combining the redox potentials of phenoxyl radicals with the aqueous acidities of phenols the bond strength of the phenolic O-H bond was calculated. These values were found to be in good agreement with O-H bond dissociation enthalpies measured in the gas phase.