56992-87-1 Usage
Description
2-Methyl-N-(4-sulfamoyl-phenyl)-acrylamide is a versatile chemical compound characterized by the presence of a sulfamoyl group attached to a phenyl ring and an acrylamide group. 2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide is recognized for its potential in organic synthesis and pharmaceutical research, where it serves as a valuable building block for the creation of diverse chemical entities. The sulfamoyl group endows it with properties that are of interest in drug development, given the known antimicrobial and biological activities of sulfonamide derivatives. Furthermore, the acrylamide group allows for participation in a broad spectrum of chemical reactions, enhancing its utility as a reagent in the preparation of an array of chemical compounds.
Uses
Used in Pharmaceutical Research:
2-Methyl-N-(4-sulfamoyl-phenyl)-acrylamide is utilized as a key intermediate in the synthesis of pharmaceutical compounds, leveraging its sulfamoyl group for potential antimicrobial properties and other biological activities. Its presence in drug candidates is attributed to the broad range of chemical reactions it can undergo, facilitating the development of new therapeutic agents.
Used in Organic Synthesis:
In the realm of organic synthesis, 2-Methyl-N-(4-sulfamoyl-phenyl)-acrylamide is employed as a versatile reagent. Its acrylamide group enables it to engage in multiple chemical reactions, making it instrumental in the preparation of a wide array of chemical compounds for various applications, including but not limited to materials science, agrochemicals, and specialty chemicals.
Used in Antimicrobial Agents Development:
2-Methyl-N-(4-sulfamoyl-phenyl)-acrylamide is used as a precursor in the development of antimicrobial agents, capitalizing on the antimicrobial potential of sulfonamide derivatives. Its unique structure allows for the design of new molecules with enhanced activity against a range of pathogens, contributing to the fight against antibiotic resistance.
Used in Chemical Reactions:
2-Methyl-N-(4-sulfaMoyl-phenyl)-acrylaMide is also used as a reactant in various chemical reactions, such as Michael additions, acylations, and other condensation reactions, due to the reactivity of the acrylamide group. This makes it a valuable component in the synthesis of complex organic molecules and polymers with specific properties tailored for industrial or research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 56992-87-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,9 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56992-87:
(7*5)+(6*6)+(5*9)+(4*9)+(3*2)+(2*8)+(1*7)=181
181 % 10 = 1
So 56992-87-1 is a valid CAS Registry Number.
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)
56992-87-1Relevant articles and documents
Method for synthesizing N-[4-(sulfonamide) phenyl] methacrylamide
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Paragraph 0055-0057, (2019/04/26)
The invention relates to the field of organic chemical synthesis, and discloses a method for synthesizing N-[4-(sulfonamide) phenyl] methacrylamide, wherein methacrylate and 4-aminobenzenesulfonamideare the materials, ethanol, tetrahydrofuran, acetone, bu
Image forming material and ammonium compound
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, (2008/06/13)
An image forming material includes an image forming layer containing a water-insoluble and alkali-soluble resin, a light-heat converting agent and a compound represented by the following general formula (1). In general formula (1), R1 to R
SYNTHESIS OF METHACRYLIC ESTERS AND AMIDES CONTAINING ANTIMICROBIAL GROUPS.
Gorchakova,Budzan,Andronova,Kolokolov,Virnik
, p. 1038 - 1041 (2007/10/02)
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
