352-15-8

Basic information

• Product Name: 4-Nitrofluorobenzol
• Synonyms: 4-Nitrofluorobenzol;Benzene, 1-fluoro-4-nitroso-
• CAS NO: 352-15-8
• Molecular Formula: C₆H₄FNO
• Molecular Weight: 125.1
• Mol File: 352-15-8.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Nitrofluorobenzol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Nitrofluorobenzol(352-15-8)
• EPA Substance Registry System: 4-Nitrofluorobenzol(352-15-8)

Safety Data

• Hazardous Substances Data: 352-15-8(Hazardous Substances Data)

Usage

General Description

4-Nitrofluorobenzene is an organic compound with the chemical formula C6H4FNO2. It is a pale yellow solid that is insoluble in water and has a melting point of 48 degrees Celsius. 4-Nitrofluorobenzene is commonly used as a precursor in the synthesis of various chemicals and pharmaceuticals, as well as a reagent in organic reactions. It is considered to be toxic and harmful if swallowed, inhaled, or in contact with skin, and may cause irritation to the respiratory system and skin. Additionally, it is classified as a hazardous substance and must be handled with care.

Upstream product

• 371-40-4 4-fluoroaniline 
• 455-17-4 (p-fluorophenyl)trimethylsilane 
• 1765-93-1 4-fluoroboronic acid 
• 350-46-9 4-Fluoronitrobenzene 

Downstream Products

• 2802-96-2 N,O-bis-(1-cyano-1-methyl-ethyl)-N-(4-fluoro-phenyl)-hydroxylamine 
• 24560-30-3 4'Fluor-4-chlor-3-nitro-azobenzol 
• 51788-96-6 (E)-(4-fluorophenyl)-(4-iodophenyl)diazene 
• 1292800-94-2 C₁₂H₁₄FNO₂ 
• 39769-33-0 (4-Chloro-phenyl)-(4-fluoro-phenyl)-diazene 
• 94664-77-4 (Z)-N-(4-fluorophenyl)-1-phenylmethanimine oxide 
• 326-04-5 1,2-bis(4-fluorophenyl)diazene oxide 
• 332-07-0 bis-(4-fluorophenyl)diazene 
• 371-40-4 4-fluoroaniline 

Relevant articles and documents

Solution Dynamics of Redox Noninnocent Nitrosoarene Ligands: Mapping the Electronic Criteria for the Formation of Persistent Metal-Coordinated Nitroxide Radicals

(Graph Presented) The redox-noninnocence of metal-coordinated C-organo nitrosoarenes has been established on the basis of solid-state characterization techniques, but the solution-phase properties of this class of metal-coordinated radicals have been rela

Ipso-Nitrosation of arylboronic acids with chlorotrimethylsilane and sodium nitrite

Nitroso compounds are versatile reagents in synthetic organic chemistry. Herein, we disclose a feasible protocol for the ipso-nitrosation of aryl boronic acids using chlorotrimethylsilane-sodium nitrite unison as nitrosation reagent system.

Structural investigations of C-nitrosobenzenes. Part 1. Solution state 1H NMR studies

Ambient and low temperature 1H NMR spectra of a wide range of 3- and 4-monosubstituted, and some di- and tri-substituted C-nitrosobenzenes have enabled -N=O substituent constants for the static and rotating ring molecules to be calculated. This has provided information on the shielding anisotropy of the N=O group which in turn leads to the firm identification of the monomeric and dimeric solution species. In all cases lowering the solution temperature enhances the relative populations of dimers to monomers, with the (Z)-azodioxy dimer being preferred over the (E)-form, irrespective of the nature of the solid state dimeric structure.