6302-58-5

Basic information

• Product Name: 4-chloro-2,6-dinitrophenyl methyl ether
• Synonyms: 5-Chloro-2-methoxy-1,3-dinitrobenzene; benzene, 5-chloro-2-methoxy-1,3-dinitro-
• CAS NO: 6302-58-5
• Molecular Formula: C₇H₅ClN₂O₅
• Molecular Weight: 232.578
• Mol File: 6302-58-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 346.9°C at 760 mmHg
• Flash Point: 163.6°C
• Density: 1.56g/cm³
• Vapor Pressure: 0.000112mmHg at 25°C
• Refractive Index: 1.598
• CAS DataBase Reference: 4-chloro-2,6-dinitrophenyl methyl ether(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-2,6-dinitrophenyl methyl ether(6302-58-5)
• EPA Substance Registry System: 4-chloro-2,6-dinitrophenyl methyl ether(6302-58-5)

Safety Data

• Hazardous Substances Data: 6302-58-5(Hazardous Substances Data)

Upstream product

• 3698-57-5 5-Chlor-1,2,3-trinitrobenzol 
• 124-41-4 sodium methylate 
• 106-48-9 4-chloro-phenol 
• 623-12-1 4-chloromethoxybenzene 
• 89-21-4 4-chloro-2-nitroanisole 
• 2213-82-3 2,5-dichloro-1,3-dinitrobenzene 
• 67-56-1 methanol 
• 74-88-4 methyl iodide 

Downstream Products

• 88-87-9 4-chloro-2,6-dinitrophenol 
• 122252-13-5 4-chloro-2,6-dinitro-(2', 3'-dihydroxy-propyl)aniline 
• 854246-54-1 N,N'-bis-(4-chloro-2,6-dinitro-phenyl)-N,N'-dinitro-ethylenediamine 
• 5388-62-5 4-chloro-2,6-dinitroaniline 
• 61511-72-6 N-Butyl-2,6-dinitro-4-chlor-anilin 
• 82366-51-6 N-(2'-cyanoethyl)-4-chloro-2,6-dinitroaniline 
• 854649-64-2 N,N'-bis-(4-chloro-2,6-dinitro-phenyl)-propanediyldiamine 
• 873420-56-5 N,N'-bis-(4-chloro-2,6-dinitro-phenyl)-ethylenediamine 
• 74718-99-3 N-ethyl-4-chloro-2,6-dinitro-aniline 

Relevant articles and documents

Kinetic studies of the reactions of some phenols and alkyl aryl ethers with dinitrogen pentoxide in perfluorocarbon solvents

The reaction of dinitrogen pentoxide in perfluorocarbon solvents with phenols and alkyl aryl ethers carrying halogeno ring-substituents results in nitrodehydrogenation. Rate measurements show that the preferred orientation of nitration is ortho > para > meta to the hydroxy group; the kinetic isotope effect, kH/kD, has a value close to unity. Phenols show considerably higher reactivity than similarly substituted alkyl phenyl ethers, and a mechanism is suggested involving initial interaction of N2O5 with the hydroxy function followed by reaction via cyclic transition states.