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29682-41-5

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29682-41-5 Usage

Description

1,4-Dichloro-2-iodobenzene is an organic compound with the chemical formula C6H3Cl2I. It is a clear, colorless to brownish liquid and is known for its chemical properties that make it suitable for various applications in different industries.

Uses

Used in Chemical Synthesis:
1,4-Dichloro-2-iodobenzene is used as a chemical intermediate for the synthesis of thioether bond-containing aromatic diamines. Its unique chemical structure allows it to be a valuable component in the creation of these specific types of compounds, which can have various applications in the chemical and pharmaceutical industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 1,4-dichloro-2-iodobenzene can be used as a building block for the development of new drugs. Its chemical properties make it a versatile compound that can be modified and incorporated into various drug molecules, potentially leading to the discovery of novel therapeutic agents.
Used in Dye and Pigment Industry:
1,4-Dichloro-2-iodobenzene can also be utilized in the dye and pigment industry as a starting material for the synthesis of various organic dyes and pigments. Its unique chemical structure can contribute to the development of new colorants with improved properties, such as enhanced color strength, stability, and resistance to fading.
Used in Polymer Industry:
In the polymer industry, 1,4-dichloro-2-iodobenzene can be used as a monomer or a building block for the synthesis of specialty polymers. These polymers can have specific properties, such as improved thermal stability, chemical resistance, or mechanical strength, making them suitable for various applications, including coatings, adhesives, and plastics.
Used in Analytical Chemistry:
1,4-Dichloro-2-iodobenzene can be employed as a reference compound or a standard in analytical chemistry. Its distinct chemical properties can be used to calibrate instruments, validate analytical methods, or serve as a benchmark for comparing the performance of different analytical techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 29682-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,8 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29682-41:
(7*2)+(6*9)+(5*6)+(4*8)+(3*2)+(2*4)+(1*1)=145
145 % 10 = 5
So 29682-41-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl2I/c7-4-1-2-5(8)6(9)3-4/h1-3H

29682-41-5 Well-known Company Product Price

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  • Alfa Aesar

  • (A14172)  1,4-Dichloro-2-iodobenzene, 98%   

  • 29682-41-5

  • 10g

  • 336.0CNY

  • Detail
  • Alfa Aesar

  • (A14172)  1,4-Dichloro-2-iodobenzene, 98%   

  • 29682-41-5

  • 50g

  • 1184.0CNY

  • Detail
  • Alfa Aesar

  • (A14172)  1,4-Dichloro-2-iodobenzene, 98%   

  • 29682-41-5

  • 250g

  • 4739.0CNY

  • Detail

29682-41-5SDS

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 1,4-DICHLORO-2-IODOBENZENE

1.2 Other means of identification

Product number -
Other names 2,5-Dichloroiodobenzene

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:29682-41-5 SDS

29682-41-5Relevant articles and documents

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Dains,Magers

, p. 1572 (1930)

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General copper-catalyzed transformations of functional groups from arylboronic acids in water

Yang, Haijun,Li, Yong,Jiang, Min,Wang, Junmei,Fu, Hua

experimental part, p. 5652 - 5660 (2011/06/23)

A simple and general copper-catalyzed method has been developed for transformations of various functional groups (i I, i N3, i SO2R, i OH, i NH2, and i NO 2) on aromatic rings from arylboronic acids in water under air. The protocol uses cheap and readily available inorganic salts (KI, NaN3, NaSO2R, NaOH, NaNO2) and aqueous ammonia as the functional-group sources, simple Cu2O/NH3 as the catalyst system, environmentally friendly water as the solvent, and oxygen in air as the oxidant. Importantly, the copper catalyst system in water was recyclable. This study should provide a useful strategy for interconversions of the functional groups on aromatic rings.

Synthesis of Chlorinated and Brominated Biphenyl Oxides

Reich, Ieva L.,Reich, Hans J.

, p. 3721 - 3727 (2007/10/02)

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