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696-02-6

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696-02-6 Usage

Description

1-Chloro-3,4-difluorobenzene is an organic compound with the chemical formula C6H2ClF2. It is a derivative of benzene, featuring one chlorine atom and two fluorine atoms attached to the benzene ring. 1-Chloro-3,4-difluorobenzene is known for its unique chemical properties and potential applications in various industries.

Uses

Used in Chemical Synthesis:
1-Chloro-3,4-difluorobenzene is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its presence of chlorine and fluorine atoms allows for further functionalization and the formation of a wide range of derivatives.
Used in Pharmaceutical Industry:
1-Chloro-3,4-difluorobenzene is used as a building block for the development of new drugs and pharmaceutical agents. Its unique structure and reactivity make it a valuable component in the design and synthesis of novel therapeutic agents.
Used in Agrochemical Industry:
1-Chloro-3,4-difluorobenzene is used as a precursor in the production of agrochemicals, such as insecticides, herbicides, and fungicides. Its chemical properties enable the development of effective and targeted pest control solutions.
Used in Dye and Pigment Industry:
1-Chloro-3,4-difluorobenzene is used as a starting material for the synthesis of dyes and pigments. Its ability to form various derivatives allows for the creation of a diverse range of colorants for use in various applications, such as textiles, plastics, and printing inks.
Used in Preparation of 1-Chloro-4,5-difluoro-2-nitrobenzene:
1-Chloro-3,4-difluorobenzene is used as a reactant in the preparation of 1-chloro-4,5-difluoro-2-nitrobenzene, which is an important compound for further chemical transformations and applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 696-02-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 696-02:
(5*6)+(4*9)+(3*6)+(2*0)+(1*2)=86
86 % 10 = 6
So 696-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClF2/c7-4-1-2-5(8)6(9)3-4/h1-3H

696-02-6 Well-known Company Product Price

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  • Alfa Aesar

  • (A12924)  4-Chloro-1,2-difluorobenzene, 98%   

  • 696-02-6

  • 5g

  • 236.0CNY

  • Detail
  • Alfa Aesar

  • (A12924)  4-Chloro-1,2-difluorobenzene, 98%   

  • 696-02-6

  • 25g

  • 983.0CNY

  • Detail
  • Alfa Aesar

  • (A12924)  4-Chloro-1,2-difluorobenzene, 98%   

  • 696-02-6

  • 100g

  • 3121.0CNY

  • Detail

696-02-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Chloro-3,4-difluorobenzene

1.2 Other means of identification

Product number -
Other names 1-Chloro-3,4-difluorobenzene

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:696-02-6 SDS

696-02-6Relevant articles and documents

Three-step regioselective synthesis of 2,3-difluorohalobenzenes using tetrafluoroethylene and buta-1,3-diene as starting building blocks

Egorov, M. P.,Lipkind, M. B.,Nefedov, O. M.,Volchkov, N. V.

, p. 925 - 932 (2021/06/07)

The gas-phase copyrolysis of tetrafluoroethylene and buta-1,3-diene in a flow tube reactor at 490–510 °C gives 3,3,4,4-tetrafluorocyclohex-1-ene, which is selectively converted to 1-bromo- or 1-chloro-2,3-difluorobenzene via intermediate steps of halogenation and dehydrohalogenation.

Method for producing tetrakis ( fluoroaryl) borate-magnesium compound

-

, (2008/06/13)

Fluoroaryl magnesium halide is reacted with a boron compound so that a molar ratio of the fluoroaryl magnesium halide to the boron compound is not less than 3.0 and not more than 3.7, so as to produce a tetrakis (fluoroaryl) borate·magnesium compound. With this method, there occurs no hydrogen fluoride which corrodes a producing apparatus and requires troublesome waste water treatment.

Process for producing chlorofluorobenzenes

-

, (2008/06/13)

A process for producing chlorofluorobenzenes, which comprises reacting fluorine-containing nitrobenzenes of the following formula (1) with chlorine gas to obtain chlorofluorobenzenes of the following formula (2): STR1 wherein n and m are integers satisfying 1≤n≤3, 0≤m≤2 and 1≤n+m≤3.

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