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2050-66-0

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2050-66-0 Usage

Description

2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE, also known as Bis(4-Chloro-2-nitrophenyl) Disulfide, is an organic compound with the molecular formula C12H6Cl2N2O4S2. It is characterized by its disulfide bond and the presence of nitro and chloro substituents on the phenyl rings. 2,2'-DINITRO-4,4'-DICHLORO DIPHENYL DISUFIDE is known for its chemical reactivity and potential applications in various industries.

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.

Check Digit Verification of cas no

The CAS Registry Mumber 2050-66-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2050-66:
(6*2)+(5*0)+(4*5)+(3*0)+(2*6)+(1*6)=50
50 % 10 = 0
So 2050-66-0 is a valid CAS Registry Number.
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

2050-66-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-1-[(4-chloro-2-nitrophenyl)disulfanyl]-2-nitrobenzene

1.2 Other means of identification

Product number -
Other names 2,2'-Dinitro-4,4'-dichloro diphenyl disufide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2050-66-0 SDS

2050-66-0Relevant articles and documents

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

Margolis, Brandon J.,Swidorski, Jacob J.,Rogers, Bruce N.

, p. 644 - 647 (2007/10/03)

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.

PREPARATION AND STUDY OF THE PHYTOHORMONIC ACTIVITY OF ARYLTHIOALKANOIC ACIDS AND THEIR AMIDES.

PONCI,BARUFFINI,BORGNA

, p. 356 - 376 (2007/10/06)

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