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68325-15-5

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68325-15-5 Usage

Description

3-Chloro-4-cyanopyridine, with the CAS number 68325-15-5, is a pale yellow solid compound that is widely utilized in the field of organic synthesis. It is known for its unique chemical properties, which make it a valuable component in the creation of various chemical compounds and materials.

Uses

Used in Organic Synthesis:
3-Chloro-4-cyanopyridine is used as a key intermediate for the synthesis of various organic compounds. Its application is primarily due to its unique chemical structure, which allows for the formation of a wide range of products through different chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-Chloro-4-cyanopyridine is used as a building block for the development of new drugs. Its chemical properties make it suitable for the creation of molecules with potential therapeutic applications, contributing to the advancement of medical treatments.
Used in Agrochemical Industry:
3-Chloro-4-cyanopyridine is also utilized in the agrochemical industry for the synthesis of various pesticides and other chemical products used in agriculture. Its role in this industry is to provide a foundation for the development of compounds that can help protect crops and enhance agricultural productivity.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 3-Chloro-4-cyanopyridine is employed as a starting material for the production of various dyes and pigments. Its unique chemical properties enable the creation of a diverse range of colorants used in different applications, such as textiles, plastics, and printing inks.
Used in Chemical Research:
3-Chloro-4-cyanopyridine is also used in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic pathways. Its versatility in undergoing different chemical transformations makes it an invaluable tool for researchers in the field of chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 68325-15-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,3,2 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68325-15:
(7*6)+(6*8)+(5*3)+(4*2)+(3*5)+(2*1)+(1*5)=135
135 % 10 = 5
So 68325-15-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H3ClN2/c7-6-4-9-2-1-5(6)3-8/h1-2,4H

68325-15-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H27187)  3-Chloro-4-cyanopyridine, 95%   

  • 68325-15-5

  • 1g

  • 5635.0CNY

  • Detail
  • Alfa Aesar

  • (H27187)  3-Chloro-4-cyanopyridine, 95%   

  • 68325-15-5

  • 5g

  • 12995.0CNY

  • Detail

68325-15-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Chloro-4-cyanopyridine

1.2 Other means of identification

Product number -
Other names 3-chloropyridine-4-carbonitrile

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:68325-15-5 SDS

68325-15-5Relevant articles and documents

C?H Cyanation of 6-Ring N-Containing Heteroaromatics

Elbert, Bryony L.,Farley, Alistair J. M.,Gorman, Timothy W.,Johnson, Tarn C.,Genicot, Christophe,Lallemand, Bénédicte,Pasau, Patrick,Flasz, Jakub,Castro, José L.,MacCoss, Malcolm,Paton, Robert S.,Schofield, Christopher J.,Smith, Martin D.,Willis, Michael C.,Dixon, Darren J.

supporting information, p. 14733 - 14737 (2017/10/07)

Heteroaromatic nitriles are important compounds in drug discovery, both for their prevalence in the clinic and due to the diverse range of transformations they can undergo. As such, efficient and reliable methods to access them have the potential for far-reaching impact across synthetic chemistry and the biomedical sciences. Herein, we report an approach to heteroaromatic C?H cyanation through triflic anhydride activation, nucleophilic addition of cyanide, followed by elimination of trifluoromethanesulfinate to regenerate the cyanated heteroaromatic ring. This one-pot protocol is simple to perform, is applicable to a broad range of decorated 6-ring N-containing heterocycles, and has been shown to be suitable for late-stage functionalization of complex drug-like architectures.

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