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113571-15-6

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113571-15-6 Usage

Description

4,6-DIBROMO-2,3-DICHLOROANILINE is a bromination product of dichloro-substituted aniline, characterized by its beige solid appearance. It is a chemical compound that has undergone a specific substitution process, resulting in a unique structure with potential applications in various industries.

Uses

Used in Chemical Synthesis:
4,6-DIBROMO-2,3-DICHLOROANILINE is used as an intermediate in the chemical synthesis process for the preparation of benzothiazoles. Benzothiazoles are important compounds with a wide range of applications, including pharmaceuticals, dyes, and other industrial chemicals. The unique structure of 4,6-DIBROMO-2,3-DICHLOROANILINE makes it a valuable component in the synthesis of these versatile compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,6-DIBROMO-2,3-DICHLOROANILINE is used as a building block for the development of new drugs. Its specific chemical properties allow it to be incorporated into the molecular structure of various pharmaceutical compounds, potentially enhancing their efficacy and therapeutic properties.
Used in Dye Industry:
4,6-DIBROMO-2,3-DICHLOROANILINE is also utilized in the dye industry for the production of various types of dyes. Its unique chemical structure contributes to the color properties of the dyes, making it a valuable component in the creation of a diverse range of colorants for various applications.
Used in Research and Development:
In addition to its practical applications, 4,6-DIBROMO-2,3-DICHLOROANILINE is also used in research and development for the study of chemical reactions and the development of new synthetic methods. Its unique properties make it an interesting subject for scientific investigation, potentially leading to new discoveries and advancements in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 113571-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,7 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 113571-15:
(8*1)+(7*1)+(6*3)+(5*5)+(4*7)+(3*1)+(2*1)+(1*5)=96
96 % 10 = 6
So 113571-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Br2Cl2N/c7-2-1-3(8)6(11)5(10)4(2)9/h1H,11H2

113571-15-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A14961)  4,6-Dibromo-2,3-dichloroaniline, 98%   

  • 113571-15-6

  • 1g

  • 145.0CNY

  • Detail
  • Alfa Aesar

  • (A14961)  4,6-Dibromo-2,3-dichloroaniline, 98%   

  • 113571-15-6

  • 5g

  • 517.0CNY

  • Detail

113571-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-DIBROMO-2,3-DICHLOROANILINE

1.2 Other means of identification

Product number -
Other names -

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:113571-15-6 SDS

113571-15-6Upstream product

113571-15-6Downstream Products

113571-15-6Relevant articles and documents

Identification of bromination products of chloro-substituted anilines in aqueous environment by gas chromatography

Gruzdev,Filippova,Zenkevich,Kondratenok

experimental part, p. 1748 - 1759 (2012/02/15)

To reduce the detection limits of aniline and its various chloroderivatives (all isomers of mono- and dichloroanilines, 2,4,5 -, 2,4,6-, and 3,4,5-trichloroanilines, pentachloroaniline) in aqueous media we suggested bromination reaction, followed by gas chromatographic definition bromo derivatives of chloroanilines on a selective electron capture detector. To identify the products of bromination of chloroaniline in combination with mass-spectrometric data we used chromatographic retention indices on standard nonpolar polydimethylsiloxane stationary phase that was determined for 50 compounds in this class. The technique of identifying bromoderivatives of chloroaniline in water was developed at the gas-chromatographic analysis in the selective electron capture detector. To improve the reliability of the identification of additional bromoderivatives of chloroanilines we obtained their trifluoroacetyl derivatives.

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