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2-(3-fluoro-4-nitrophenyl)propanenitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85397-18-8

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85397-18-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85397-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,9 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 85397-18:
(7*8)+(6*5)+(5*3)+(4*9)+(3*7)+(2*1)+(1*8)=168
168 % 10 = 8
So 85397-18-8 is a valid CAS Registry Number.

85397-18-8Downstream Products

85397-18-8Relevant academic research and scientific papers

(AZA)INDOLE-, BENZOTHIOPHENE-, AND BENZOFURAN-3-SULFONAMIDES

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Page/Page column 209, (2018/07/29)

Disclosed are sulfonamide compounds with GPR17 modulating properties, which are useful for treating or preventing a variety of CNS and other diseases, in particular for preventing and treating myelinating diseases or disorders.

Nucleophilic substitution process

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, (2008/06/13)

In a process for preparing a 2-(fluoronitrobenzene)acetonitrile by reacting a fluoronitrobenzene with an alpha,alpha-disubstituted acetonitrile in an inert solvent and in the presence of a base, the temperature is maintained not higher than about 15° C. t

Vicarious Nucleophilic Substitution of Hydrogen in Nitroarenes with α-Substituted Nitriles and Esters. Direct α-Cyanoalkylation and α-Carbalkoxyalkylation of Nitroarenes

Makosza, Mieczyslaw,Winiarski, Jerzy

, p. 1494 - 1499 (2007/10/02)

Carbanions generated from alkanenitriles bearing α-chloro, α-OR, or α-SR groups and from aliphatic esters bearing α-SR groups react with mononitroarenes to replace hydrogen atoms of the nitroaromatic ring ortho or para to the nitro group with α-cyanoalkyl or α-carbalkoxyalkyl substituents.The nucleophilic replacement of hydrogen with such carbanions proceeds faster than substitution of halogen ortho or para to the nitro group.

Nucleophilic substitution process

-

, (2008/06/13)

2-(Fluoronitrobenzene)alkyl cyanides are prepared by reacting a fluoronitrobenzene with an alpha-substituted alkyl cyanide in a substantially anhydrous aprotic solvent and in the presence of a base so that the alkyl cyanide reactant undergoes a nucleophil

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