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2-(4-Benzoylphenoxy)-5-nitrobenzonitrile is a complex organic chemical compound characterized by its molecular formula C20H12N2O4. 2-(4-benzoylphenoxy)-5-nitrobenzonitrile features a benzonitrile core, which is a benzene ring with a nitrile group (C≡N) attached to it. The molecule is further adorned with a 4-benzoylphenoxy group, which is a phenol derivative where one of the hydrogen atoms on the phenol ring is replaced by a benzoyl group (a benzene ring with a carbonyl group). Additionally, the compound has a nitro group (-NO2) attached to the benzonitrile core, which contributes to its reactivity and properties. This chemical is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, although its specific uses and properties would depend on the context in which it is being considered.

78940-72-4

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78940-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78940-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,4 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 78940-72:
(7*7)+(6*8)+(5*9)+(4*4)+(3*0)+(2*7)+(1*2)=174
174 % 10 = 4
So 78940-72-4 is a valid CAS Registry Number.

78940-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-benzoylphenoxy)-5-nitrobenzonitrile

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78940-72-4 SDS

78940-72-4Downstream Products

78940-72-4Relevant academic research and scientific papers

Antipicornavirus activity of substituted phenoxybenzenes and phenoxypyridines

Markley,Tong,Dulworth,Steward,Goralski,Johnston,Wood,Vinogradoff,Bargar

, p. 427 - 433 (2007/10/02)

Phenoxybenzenes and phenoxypyridines were prepared and tested for the effect of substituents on antipicornavirus activity. The most active compound, 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (8), demonstrated broad-spectrum antipicornavirus activity. Co

Substituted benzonitriles having antiviral activity

-

, (2008/06/13)

Substituted benzonitriles having antiviral activity are disclosed. Methods of use based on the antiviral activity of the compounds are also disclosed, as well as compositions which comprise a carrier in combination with a suitable antiviral active compoun

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