364-32-9

Basic information

• Product Name: 2,6-DINITRO-4-FLUOROPHENOL
• Synonyms: 2,6-DINITRO-4-FLUOROPHENOL;4-FLUORO-2,6-DINITROPHENOL;4-FLUORO-2,6-DINITROPHENOL 97%;Phenol, 4-fluoro-2,6-dinitro-;2,6-Dinitro-4-fluorophenol98%
• CAS NO: 364-32-9
• Molecular Formula: C₆H₃FN₂O₅
• Molecular Weight: 202.1
• Mol File: 364-32-9.mol
• Article Data: 16

Chemical Properties

• Melting Point: 54-56°C
• Boiling Point: 255.6°Cat760mmHg
• Flash Point: 108.4°C
• Appearance: /
• Density: 1.745g/cm³
• Vapor Pressure: 0.0101mmHg at 25°C
• PKA: 2.96±0.10(Predicted)
• CAS DataBase Reference: 2,6-DINITRO-4-FLUOROPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DINITRO-4-FLUOROPHENOL(364-32-9)
• EPA Substance Registry System: 2,6-DINITRO-4-FLUOROPHENOL(364-32-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 364-32-9(Hazardous Substances Data)

Usage

General Description

2,6-Dinitro-4-Fluorophenol is a chemical compound that is typically used in various scientific and industrial applications. As the name suggests, it comprises nitro and phenol groups, which contribute to its chemical properties. 2,6-DINITRO-4-FLUOROPHENOL is often recognized for its unique configuration of functional groups, which make it reactive and versatile in various chemical reactions. It is a pale yellow to brown solid that is sensitive to light. It is also slightly soluble in water and emits toxic fumes of nitrogen oxides, fluorides, and various other toxic compounds when heated. As a toxic and hazardous substance, it must be handled with proper safety measures.

InChI:InChI=1/C6H3FN2O5/c7-3-1-4(8(11)12)6(10)5(2-3)9(13)14/h1-2,10H/p-1

Upstream product

• 459-60-9 1-fluoro-4-methoxybenzene 
• 371-41-5 4-Fluorophenol 
• 462-06-6 fluorobenzene 
• 459-26-7 4-ethoxy-1-fluorobenzene 
• 123871-59-0 4-fluoro-4-nitrocyclohexa-2,5-dienone 
• 3324-58-1 sodium picrate 
• 405-51-6 4-fluorophenyl acetate 
• 7664-93-9 sulfuric acid 
• 7697-37-2 nitric acid 

Downstream Products

• 342-49-4 2,6-dinitro-4-fluoroanisole 
• 82366-44-7 4-Fluoro-2,6-dinitroaniline 
• 7308-45-4 4-fluoro-2,6-dinitro-phenol; potassium-compound 
• 950519-74-1 5-amino-7-fluoroquinolin-2(1H)-one 
• 68200-49-7 Dimethyl-thiocarbamic acid S-[2-(2-dimethylcarbamoylsulfanyl-5-fluoro-3-nitro-phenyldisulfanyl)-4-fluoro-6-nitro-phenyl] ester 
• 100-02-7 4-nitro-phenol 
• 123871-66-9 4-Fluoro-2,4,6-trinitro-cyclohexa-2,5-dienone 
• 62558-39-8 2-chloro-5-fluoro-1,3-dinitro-benzene 

Relevant articles and documents

Crossing the insulator-to-metal barrier with a thiazyl radical conductor

The layered-sheet architecture of the crystal structure of the fluoro-substituted oxobenzene-bridged bisdithiazolyl radical FBBO affords a 2D π-electronic structure with a large calculated bandwidth. The material displays high electrical conductivity for

A Synthetic Pathway to Substituted Benzofuroxans through the Intermediacy of Sulfonates: The Case Example of Fluoro-Nitrobenzofuroxans

Benzofuroxans are well known compounds that continue to attract particular attention since the discovery of 4,6-dinitrobenzofuroxan (DNBF) back in 1899. It has been shown that these compounds possess biological activities that are related to their electro

Synthesis of 6-aminobenzopentathiepines by reactions of 4-nitrobenzodithiol-2-ones with NaHS

The reactions of benzodithiol-2-ones containing a 4-nitro group with NaHS led to mixtures of 6- aminobenzopentathiepines and 4-nitrobenzotrithiols. The product ratio and yields depend on the substituent in the aromatic ring. Based on the yields of benzopentathiepines, the following series of substituent efficiency can be inferred: CF3 ? F, Cl > CN. Aminobenzopentathiepines are probably formed via the intermediate benzotrithiols; the transformation apparently starts with the reduction of the nitro group.