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N-(4-Anilinophenyl)-methacrylamide is a chemical compound that belongs to the class of organic compounds known as methacrylamides. These compounds are amides of methacrylic acid, which are derived from methacrylic acid through the replacement of the hydroxyl group by an amine residue. N-(4-Anilinophenyl)-methacrylamide has been utilized in research studies for its diverse properties, particularly in the preparation of polymers. It is widely recognized as a valuable compound in the fields of chemistry and material science.

41543-92-4

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41543-92-4 Usage

Uses

Used in Polymer Synthesis:
N-(4-Anilinophenyl)-methacrylamide is used as a monomer in the synthesis of polymers for various applications. Its unique chemical structure allows for the creation of polymers with specific properties, such as improved mechanical strength, thermal stability, and chemical resistance.
Used in Research Studies:
In the field of chemistry and material science, N-(4-Anilinophenyl)-methacrylamide is used as a research compound to explore its properties and potential applications. It has been employed in studies to understand its reactivity, polymerization behavior, and interactions with other compounds.
Used in Chemical Industry:
N-(4-Anilinophenyl)-methacrylamide is utilized in the chemical industry for the development of new materials and products. Its versatile chemical properties make it suitable for use in the synthesis of various chemical intermediates, coatings, adhesives, and other specialty chemicals.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its potential for polymer synthesis and interaction with other compounds, N-(4-Anilinophenyl)-methacrylamide could be used in the pharmaceutical industry for the development of drug delivery systems, targeting specific biological pathways, or as a component in the synthesis of new pharmaceutical agents.

Check Digit Verification of cas no

The CAS Registry Mumber 41543-92-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,5,4 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41543-92:
(7*4)+(6*1)+(5*5)+(4*4)+(3*3)+(2*9)+(1*2)=104
104 % 10 = 4
So 41543-92-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H16N2O/c1-12(2)16(19)18-15-10-8-14(9-11-15)17-13-6-4-3-5-7-13/h3-11,17H,1H2,2H3,(H,18,19)

41543-92-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-anilinophenyl)-2-methylprop-2-enamide

1.2 Other means of identification

Product number -
Other names EINECS 255-432-4

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:41543-92-4 SDS

41543-92-4Downstream Products

41543-92-4Relevant academic research and scientific papers

Improved process for the catalyzed synthesis of N-substituted acrylamides and methacrylamides

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, (2008/06/13)

The present invention relates to an improved process for the catalyzed synthesis of N-substituted acrylamides and methacrylamides. In particular the present process involves reacting an acrylic or methacrylic acid ester with an aliphatic or an amine in th

Process for preparing aromatic amide antioxidants

-

, (2008/06/13)

A process for the preparation of aromatic amide antioxidants from a simple aliphatic or aromatic ester and primary amine in the presence of a metal alkoxide and an alcohol. Unsaturated products produced using this process are sufficiently pure to use as c

Process for the preparation of antioxidant amides

-

, (2008/06/13)

An inexpensive and nonhazardous process for the preparation of an amide wherein an organic acid reacting with an aryl amine to form an intermediate hydroxy aryl amide and then dehydrating the hydroxy aryl amide to form a α, β unsaturated amide.

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