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(2E)-2-[4-(dimethylamino)phenyl]imino-3-(4-methylphenyl)-3-oxopropanenitrile is a yellow solid compound with the molecular formula C20H19N3O. It is a versatile organic compound commonly used in organic synthesis and chemical research due to its reactivity and potential applications in the pharmaceutical industry. (2E)-2-[4-(dimethylamino)phenyl]imino-3-(4-methylphenyl)-3-oxopropanenitrile features a nitrile functional group, making it a valuable building block for the synthesis of various organic compounds. Its structure includes a benzene ring substituted with dimethylamino and methylphenyl groups, with an imine and nitrile functional group attached to a 3-oxopropanenitrile backbone. (2E)-2-[4-(dimethylamino)phenyl]imino-3-(4-methylphenyl)-3-oxopropanenitrile has the potential to be further modified to create new derivatives with tailored properties for specific applications.

23071-56-9

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23071-56-9 Usage

Uses

Used in Organic Synthesis:
(2E)-2-[4-(dimethylamino)phenyl]imino-3-(4-methylphenyl)-3-oxopropanenitrile is used as a building block in organic synthesis for the creation of various organic compounds. Its nitrile functional group allows for versatile reactivity, making it a valuable component in the synthesis of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2E)-2-[4-(dimethylamino)phenyl]imino-3-(4-methylphenyl)-3-oxopropanenitrile is used as a starting material for the development of new drugs. Its unique structure and functional groups can be further modified to create derivatives with specific properties, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
(2E)-2-[4-(dimethylamino)phenyl]imino-3-(4-methylphenyl)-3-oxopropanenitrile is also utilized in chemical research to study the properties and reactions of various functional groups. Its reactivity and structural features make it an interesting subject for exploration in academic and industrial research settings.

Check Digit Verification of cas no

The CAS Registry Mumber 23071-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,7 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23071-56:
(7*2)+(6*3)+(5*0)+(4*7)+(3*1)+(2*5)+(1*6)=79
79 % 10 = 9
So 23071-56-9 is a valid CAS Registry Number.

23071-56-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(dimethylamino)phenyl]-2-(4-methylphenyl)-2-oxoethanimidoyl cyanide

1.2 Other means of identification

Product number -
Other names N-(4-dimethylaminophenyl)-2-(4-methylphenyl)-2-oxoethanimidoyl cyanide

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:23071-56-9 SDS

23071-56-9Downstream Products

23071-56-9Relevant academic research and scientific papers

Reactions of α-Ketoazides with N,N-Dimethylamino-nitrosobenzol. Synthesis of α-Imino-β-Ketonitriles and their Redox Properties

Knittel, Dierk

, p. 930 - 933 (2007/10/02)

A survey about the reaction between α-azidoacetophenones with aromatic nitroso compounds is given.The synthesis of α-imino-β-ketonitriles and some electochemical properties of this class are described. - Key words: α-Ketoazides, Iminoketonitriles, Cathodic Reduction

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