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13714-86-8

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13714-86-8 Usage

Synthesis Reference(s)

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

General Description

5-Methyl-2-furonitrile is formed on reacting α-furfuryl chloride with strong aqueous potassium cyanide.

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

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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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