2050-66-0

Basic information

• Product Name: 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE
• Synonyms: 2,2''-DINITRO-4,4''-DICHLORODIPHENYL DISUFIDE 98%;1,1'-Dithiobis(4-chloro-2-nitrobenzene);Bis(2-nitro-4-chlorophenyl) persulfide;Bis(4-chloro-2-nitrophenyl) persulfide;4，4’-Dichloro-2,2'-dinitro diphenyl;4-chloro-2-nitrophenyl disulfide;4-chloro-1-(4-chloro-2-nitro-phenyl)disulfanyl-2-nitro-benzene;4-chloro-1-(4-chloro-2-nitrophenyl)disulfanyl-2-nitrobenzene
• CAS NO: 2050-66-0
• Molecular Formula: C₁₂H₆Cl₂N₂O₄S₂
• Molecular Weight: 377.22
• EINECS: 218-094-9
• Mol File: 2050-66-0.mol

Chemical Properties

• Melting Point: 214.0 to 218.0 °C
• Boiling Point: 476.9 °C at 760 mmHg
• Flash Point: 242.2 °C
• Appearance: /
• Density: 1.68g/cm³
• Vapor Pressure: 8.42E-09mmHg at 25°C
• Refractive Index: 1.729
• CAS DataBase Reference: 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE(2050-66-0)
• EPA Substance Registry System: 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE(2050-66-0)

Safety Data

• Hazardous Substances Data: 2050-66-0(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE is used as a building block in the chemical synthesis industry for the preparation of novel benzothiazine derivatives. Its unique structure and reactivity make it a valuable component in the development of new compounds with potential applications in various fields, such as pharmaceuticals, materials science, and agrochemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE is used as an intermediate in the synthesis of various drugs and drug candidates. Its chemical properties allow for the creation of new molecules with potential therapeutic effects, contributing to the development of innovative treatments for various diseases and conditions.
Used in Materials Science:
2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE is also utilized in the materials science field for the development of new materials with specific properties. Its incorporation into polymers and other materials can lead to improved characteristics, such as enhanced stability, durability, or chemical resistance, depending on the desired application.
Used in Agrochemical Industry:
In the agrochemical industry, 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE is used as a starting material for the synthesis of various pesticides and agrochemicals. Its chemical structure can be modified to create compounds with targeted effects on pests or weeds, contributing to the development of more effective and environmentally friendly agricultural products.

InChI:InChI=1/C12H6Cl2N2O4S2/c13-7-1-3-11(9(5-7)15(17)18)21-22-12-4-2-8(14)6-10(12)16(19)20/h1-6H

Upstream product

• 36776-27-9 4-chloro-2-nitro-thiophenol 
• 2719-66-6 4-chloro-2-nitro-benzenesulfinic acid 
• 95073-27-1 4-chloro-2-nitro-benzenethiosulfonic acid S-(4-chloro-2-nitro-phenyl ester) 
• 46989-62-2 4-chloro-2-nitro-benzenesulfenic acid-(4-oxo-cyclohexa-2,5-dienylidenamide) 
• 64-19-7 acetic acid 
• 100-63-0 phenylhydrazine 
• 89-61-2 2,5-dichloronitrobenzene 
• 613-32-1 5,10-dihydrophenazine 
• 4153-06-4 4-chloro-2-nitrobenzenesulfenyl chloride 
• 71-43-2 benzene 
• 64-17-5 ethanol 
• 10034-85-2 hydrogen iodide 
• 10035-10-6 hydrogen bromide 
• 7803-49-8 hydroxylamine 

Downstream Products

• 1006-99-1 2-methyl-5-chloro-benzothiazole 
• 29241-15-4 5-chlorobenzothiadiazole 
• 4533-96-4 4-chloro-2-nitrobenzenesulfonyl chloride 
• 4153-06-4 4-chloro-2-nitrobenzenesulfenyl chloride 
• 144505-71-5 bis-(4-chloro-2-nitro-phenyl) sulfone 
• 25315-45-1 4-chloro-2-nitro-benzenesulfenyl bromide 
• 1004-00-8 4-chloro-2-aminobenzenethiol 
• 6375-61-7 (4-chloro-2-nitro-phenylsulfanyl)-acetic acid 
• 17485-33-5 5-chloro-2-(4-chlorophenyl)benzo[d]thiazole 
• 952-16-9 5-chloro-2-phenylbenzothiazole 
• 92161-46-1 5-chloro-2-(4-methoxyphenyl)-1,3-benzothiazole 
• 17485-34-6 5-chloro-2-(2,4-dichlorophenyl)benzothiazole 
• 1210054-36-6 3-[(4-chloro-2-nitrophenyl)thio]-1H-indole 
• 1346164-91-7 3-(4-chloro-2-nitrophenylthio)-1-methyl-2-phenyl-1H-indole 

Relevant articles and documents

An efficient assembly of heterobenzazepine ring systems utilizing an intramolecular palladium-catalyzed cycloamination

Azaheterocyclic compounds are interesting and medicinally relevant targets. Herein we disclose an improved synthesis into the oxazepine and thiazepine ring systems. The key step in the synthesis exploits recent advancements in the palladium-catalyzed amination reaction, which was utilized to form the seven-membered rings. General conditions for this reaction were Pd2dba3, P(t-Bu)3, NaO-t-Bu alone or with K2CO3, in toluene. The scope of the reaction was investigated, and has been shown to be effective on a variety of substrates as illustrated.

Dihydrobenz thiazine derivative and microorganism control agent

A compound represented by the formula: STR1 wherein R1 and R2 each represent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group or a trifluoromethyl group; R3 represents a hydrogen atom, a lower alkyl group, a phenyl group or a lower alkoxy-carbonyl group; R4 and R5 each represent a hydrogen atom or a lower alkyl group; R6 represents a halogen atom; and X represents an oxygen atom or a sulfur atom, and a microorganism control agent, comprising the above compound as an active ingredient.