54715-57-0

Basic information

• Product Name: 3-CHLORO-4,6-DINITROPHENOL
• Synonyms: 3-CHLORO-4,6-DINITROPHENOL
• CAS NO: 54715-57-0
• Molecular Formula: C₆H₃ClN₂O₅
• Molecular Weight: 218.55
• Mol File: 54715-57-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 92°C
• Boiling Point: 337.4°C at 760 mmHg
• Flash Point: 157.9°C
• Appearance: /
• Density: 1.7400
• Vapor Pressure: 5.36E-05mmHg at 25°C
• Refractive Index: 1.6290 (estimate)
• CAS DataBase Reference: 3-CHLORO-4,6-DINITROPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-CHLORO-4,6-DINITROPHENOL(54715-57-0)
• EPA Substance Registry System: 3-CHLORO-4,6-DINITROPHENOL(54715-57-0)

Safety Data

• Hazardous Substances Data: 54715-57-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C6H3ClN2O5/c7-3-1-6(10)5(9(13)14)2-4(3)8(11)12/h1-2,10H

Upstream product

• 108-43-0 3-monochlorophenol 
• 611-07-4 5-chloro-2-nitrophenol 
• 491-11-2 3-chloro-4-nitrophenol 
• 554-00-7 2,4-Dichloroaniline 
• 40140-91-8 3-chloro-4-nitrosophenol 
• 541-73-1 1,3-Dichlorobenzene 
• 611-06-3 2,4-dichloronitrobenzene 
• 3698-83-7 2,4-dichloro-1,5-dinitrobenzene 
• 60-35-5 acetamide 
• 7732-18-5 water 
• 127-09-3 sodium acetate 
• 97-00-7 1-chloro-2,4-dinitro-benzene 

Downstream Products

• 861338-12-7 4.6-dinitro-3.4'-dioxy-azobenzene 
• 96166-84-6 2-chloro-4,6-dinitro-N,N'-di-p-tolyl-m-phenylenediamine 
• 6379-46-0 1,2,3-trichloro-4,6-dinitrobenzene 
• 860603-32-3 3-bromo-2,4-dichloro-1,5-dinitro-benzene 
• 118353-02-9 N,N-diethyl-4-nitro-1,2-phenylenediamine 
• 55346-96-8 2,3-dichloro-4,6-dinitrophenol 
• 78697-71-9 5-(N,N-diethylamino)-2,4-dinitrophenol 
• 3698-83-7 2,4-dichloro-1,5-dinitrobenzene 
• 861338-19-4 4.6-dinitro-3-oxy-phenylhydrazine 
• 858854-80-5 3-chloro-2-iodo-4,6-dinitro-phenol 
• 858855-20-6 2-bromo-3-chloro-4,6-dinitro-phenol 

Relevant articles and documents

Hydroxylation of Nitroarenes with Alkyl Hydroperoxide Anions via Vicarious Nucleophilic Substitution of Hydrogen

Rhone-Poulenc Polska Ltd., ul. Grzybowska 80/82, 00-844 Warszawa, Poland Garbo- and heterocyclic nitroarenes react with anions of tert-butyl and cumyl hydroperoxides in the presence of strong bases to form substituted o- and p-nitrophenols. The reaction usually proceeds in high yields and is of practical value as a method of synthesis and manufacturing of nitrophenols. Orientation of the hydroxylation can be controlled to a substantial extent by selection of the proper conditions. Basic mechanistic features of this process were clarified.

Water-soluble trisazo 8-amino-naphthol-1 dyes

Very effective direct dyeing of cotton and other hydroxyl- or nitrogen-containing fibers is effected with water-soluble triasazo dyes having the formula: where A is a radical of a diazoconstituent and A3 is a radical of a coupling constituent STR1 and A1 or A2 or both can have their azo linkages reversed. These dyes are very fast particularly to washing and to perspiration, and are so effective with cotton that dye baths for such use are rapidly exhausted and the disposal of used bath is less of a problem.