56992-87-1

Basic information

• Product Name: 2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide
• Synonyms: 2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide;N-(p-aMinosulfonylphenyl)-MethacrylaMide;4-2-methyl-N-(4-sulfamoylphenyl)prop-2-enamide
• CAS NO: 56992-87-1
• Molecular Formula: C₁₀H₁₂N₂O₃S
• Molecular Weight: 240.27888
• Mol File: 56992-87-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.339g/cm³
• Refractive Index: 1.595
• PKA: 9.88±0.12(Predicted)
• CAS DataBase Reference: 2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide(56992-87-1)
• EPA Substance Registry System: 2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide(56992-87-1)

Safety Data

• Hazardous Substances Data: 56992-87-1(Hazardous Substances Data)

Usage

General Description

2-Methyl-N-(4-sulfamoyl-phenyl)-acrylamide is a chemical compound that contains a sulfamoyl group attached to a phenyl ring and an acrylamide group. It is commonly used in organic synthesis and pharmaceutical research due to its ability to act as a building block for the synthesis of various compounds. The presence of the sulfamoyl group contributes to its potential as a drug candidate, as sulfonamide derivatives have been shown to exhibit antimicrobial and other biological activities. Additionally, the acrylamide group provides this compound with the ability to participate in a variety of chemical reactions, making it a versatile reagent for the preparation of a wide range of chemical compounds.

InChI:InChI=1/C10H12N2O3S/c1-7(2)10(13)12-8-3-5-9(6-4-8)16(11,14)15/h3-6H,1H2,2H3,(H,12,13)(H2,11,14,15)

Upstream product

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Relevant articles and documents

Method for synthesizing N-[4-(sulfonamide) phenyl] methacrylamide

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SYNTHESIS OF METHACRYLIC ESTERS AND AMIDES CONTAINING ANTIMICROBIAL GROUPS.

By reacting methacryloyl (MAA) chloride with 2,4,5-trichlorophenol (TCP), pentachlorophenol (PCP), 4-aminobenzenesulfonamide (streptocid, ST), and 4-aminomethylbenzenesulfonamide (maphenide, MP) in presence of a hydrogen-chloride acceptor (dimethylformami