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13714-86-8

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13714-86-8 Usage

Description

5-Methyl-2-furonitrile, also known as tonitril, is an organic compound that is formed by reacting α-furfuryl chloride with strong aqueous potassium cyanide. It is a versatile chemical intermediate with a wide range of applications across different industries.

Uses

Used in Chemical Synthesis:
5-Methyl-2-furonitrile is used as a chemical intermediate for the synthesis of various compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for further functionalization and modification, making it a valuable building block in the chemical industry.
Used in Flavor and Fragrance Industry:
5-Methyl-2-furonitrile is used as a flavoring agent and a component in the fragrance industry. Its distinct aroma profile contributes to the creation of various scents and flavors in the production of perfumes, cosmetics, and the food and beverage industry.
Used in Polymer Industry:
In the polymer industry, 5-Methyl-2-furonitrile is used as a monomer for the production of polymers with specific properties. Its incorporation into polymer chains can enhance the material's characteristics, such as strength, flexibility, and thermal stability.
Used in Pharmaceutical Industry:
5-Methyl-2-furonitrile is used as a starting material for the synthesis of various pharmaceutical compounds. Its reactivity and functional groups make it a suitable candidate for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 5-Methyl-2-furonitrile is used as a precursor for the synthesis of pesticides, herbicides, and other crop protection agents. Its chemical properties allow for the development of effective and targeted products to improve crop yield and protect against pests and diseases.

Synthesis Reference(s)

Tetrahedron, 39, p. 3881, 1983 DOI: 10.1016/S0040-4020(01)90890-7

Check Digit Verification of cas no

The CAS Registry Mumber 13714-86-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,7,1 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13714-86:
(7*1)+(6*3)+(5*7)+(4*1)+(3*4)+(2*8)+(1*6)=98
98 % 10 = 8
So 13714-86-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H5NO/c1-5-2-3-6(4-7)8-5/h2-3H,1H3

13714-86-8 Well-known Company Product Price

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  • Aldrich

  • (524778)  5-Methyl-2-furonitrile  97%

  • 13714-86-8

  • 524778-1G

  • 820.17CNY

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13714-86-8SDS

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 5-methylfuran-2-carbonitrile

1.2 Other means of identification

Product number -
Other names 5-methyl-2-furonitrile

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:13714-86-8 SDS

13714-86-8Relevant articles and documents

Heterocyclic Adenosine Receptor Antagonists

-

Paragraph 0221-0223, (2021/09/26)

Heterocyclic compounds useful as antagonists of adenosine receptors, and methods of treatment of diseases using antagonists of adenosine receptors are disclosed herein. Also disclosed herein are pharmaceutical compositions and methods of administration of

Direct oxidative conversion of aldehydes to nitriles using IBX in aqueous ammonia

Arote, Nitin D.,Bhalerao, Dinesh S.,Akamanchi, Krishnacharya G.

, p. 3651 - 3653 (2008/02/03)

A mild, simple, chemoselective and high yielding procedure for the direct oxidative conversion of aldehydes to nitriles has been developed using IBX in aqueous ammonia.

A simple method for the synthesis of 5-substituted 2-cyanofurans

Pavlov

, p. 524 - 529 (2007/10/03)

A new method based on the Schmidt reaction was developed for the production of 5-R-2-cyanofurans from 5-R-furfurals.

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