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2-Chloro-3,4-dimethoxybenzonitrile is a chemical compound characterized by the molecular formula C9H8ClNO2. It is a pale yellow solid that serves as a versatile intermediate in the synthesis of a variety of biologically active molecules. 2-Chloro-3,4-dimethoxybenzonitrile is recognized for its utility as a building block in the development of pharmaceutical drugs, agrochemicals, and other fine chemicals. Its unique chemical and structural properties also lend it potential applications in a range of chemical and research processes.

119413-61-5

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119413-61-5 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloro-3,4-dimethoxybenzonitrile is utilized as a key intermediate in the synthesis of pharmaceutical drugs. Its chemical structure allows for the creation of a diverse array of biologically active molecules, contributing to the development of new therapeutic agents.
Used in Agrochemical Synthesis:
In the agrochemical sector, 2-Chloro-3,4-dimethoxybenzonitrile is employed as a starting material for the production of various agrochemicals. Its reactivity and structural features make it suitable for the synthesis of compounds that can be used in crop protection and other agricultural applications.
Used in the Synthesis of Heterocyclic Compounds:
2-Chloro-3,4-dimethoxybenzonitrile is also used as a starting material for the synthesis of heterocyclic compounds. These compounds are important in various fields, including pharmaceuticals, materials science, and organic synthesis, due to their diverse chemical properties and potential applications.
Used in Fine Chemicals Production:
2-Chloro-3,4-dimethoxybenzonitrile is further utilized in the production of fine chemicals, which are high-purity chemicals used in various industries, including pharmaceuticals, fragrances, and flavors. The versatility of 2-Chloro-3,4-dimethoxybenzonitrile in chemical reactions makes it a valuable component in the synthesis of these specialty chemicals.
Used in Chemical and Research Processes:
Due to its unique chemical properties, 2-Chloro-3,4-dimethoxybenzonitrile has potential applications in a variety of chemical processes and research activities. Its use can facilitate the development of new chemical methodologies and contribute to the advancement of scientific knowledge in organic chemistry and related fields.

Check Digit Verification of cas no

The CAS Registry Mumber 119413-61-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,1 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 119413-61:
(8*1)+(7*1)+(6*9)+(5*4)+(4*1)+(3*3)+(2*6)+(1*1)=115
115 % 10 = 5
So 119413-61-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClNO2/c1-12-7-4-3-6(5-11)8(10)9(7)13-2/h3-4H,1-2H3

119413-61-5 Well-known Company Product Price

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  • Alfa Aesar

  • (B20402)  2-Chloro-3,4-dimethoxybenzonitrile, 97%   

  • 119413-61-5

  • 1g

  • 218.0CNY

  • Detail
  • Alfa Aesar

  • (B20402)  2-Chloro-3,4-dimethoxybenzonitrile, 97%   

  • 119413-61-5

  • 5g

  • 845.0CNY

  • Detail

119413-61-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-CHLORO-3,4-DIMETHOXYBENZONITRILE

1.2 Other means of identification

Product number -
Other names 2-Chloro-3,4-dimethoxybenzonitrile

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:119413-61-5 SDS

119413-61-5Downstream Products

119413-61-5Relevant academic research and scientific papers

Utility of Nitrogen Extrusion of Azido Complexes for the Synthesis of Nitriles, Benzoxazoles, and Benzisoxazoles

Nimnual, Phongprapan,Tummatorn, Jumreang,Thongsornkleeb, Charnsak,Ruchirawat, Somsak

, p. 8657 - 8667 (2015)

The utility of the nitrogen extrusion reaction of azido complexes, generated in situ from the corresponding aldehydes or ketones with TMSN3 in the presence of ZrCl4 or TfOH, has been described. These azido complexes could undergo three different pathways, depending on the substrates. First, azido methanolate complexes or imine diazonium ions could lead to benzisoxazole products via an intramolecular nucleophilic substitution. Second, imine diazonium ions could also undergo either the elimination of proton to provide nitrile products in good to excellent yields or an aryl migration, followed by an intramolecular nucleophilic addition, to give benzoxazole products in good yields.

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