Cas no 1000932-96-6 (1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide)

1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide structure
1000932-96-6 structure
Product Name:1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide
CAS No:1000932-96-6
MF:C12H13N3O3S
MW:279.314921140671
MDL:MFCD09863421
CID:5055721
PubChem ID:25489689
Update Time:2025-11-02

1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide Chemical and Physical Properties

Names and Identifiers

    • 1-methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide
    • NE61142
    • 1-methyl-4-(phenylsulfamoyl)pyrrole-2-carboxamide
    • Z317436986
    • Z316912734
    • CS-0245652
    • AKOS009164697
    • EN300-30819
    • G24228
    • 1000932-96-6
    • 4-(anilinosulfonyl)-1-methyl-1H-pyrrole-2-carboxamide
    • 1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide
    • MDL: MFCD09863421
    • Inchi: 1S/C12H13N3O3S/c1-15-8-10(7-11(15)12(13)16)19(17,18)14-9-5-3-2-4-6-9/h2-8,14H,1H3,(H2,13,16)
    • InChI Key: DSUAOTKDMKUCLW-UHFFFAOYSA-N
    • SMILES: S(C1C=C(C(N)=O)N(C)C=1)(NC1C=CC=CC=1)(=O)=O

Computed Properties

  • Exact Mass: 279.06776246g/mol
  • Monoisotopic Mass: 279.06776246g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 4
  • Complexity: 426
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.4
  • Topological Polar Surface Area: 103

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Additional information on 1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide

Comprehensive Overview of 1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide (CAS No. 1000932-96-6)

1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide, identified by its CAS number 1000932-96-6, is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound belongs to the class of sulfonamide derivatives, which are widely recognized for their diverse biological activities. The unique structural features of this molecule, including the pyrrole ring and sulfamoyl group, make it a promising candidate for various applications in drug discovery and development.

In recent years, the scientific community has shown increasing interest in sulfonamide-based compounds due to their potential therapeutic benefits. Researchers are particularly focused on understanding the structure-activity relationship (SAR) of molecules like 1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide. This compound's carboxamide moiety and phenylsulfamoyl group contribute to its ability to interact with biological targets, making it a subject of study in fields such as enzyme inhibition and receptor modulation.

The synthesis of CAS 1000932-96-6 involves multi-step organic reactions, often starting with the functionalization of the pyrrole core. Advanced techniques like nuclear magnetic resonance (NMR) and high-performance liquid chromatography (HPLC) are employed to ensure the purity and structural integrity of the final product. Given the growing demand for high-purity research chemicals, this compound is often supplied under stringent quality control measures to meet the needs of academic and industrial laboratories.

One of the most frequently asked questions about 1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide revolves around its potential applications in medicinal chemistry. Preliminary studies suggest that this compound may exhibit anti-inflammatory or antimicrobial properties, aligning with the broader trend of repurposing sulfonamide scaffolds for new therapeutic uses. Additionally, its molecular weight and solubility profile make it suitable for formulation studies, which are critical for drug delivery optimization.

From an SEO perspective, keywords such as "sulfonamide pyrrole derivatives," "CAS 1000932-96-6 supplier," and "1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide uses" are highly relevant to researchers and industry professionals. These terms reflect the current focus on innovative chemical entities and their role in addressing unmet medical needs. Furthermore, discussions around green chemistry and sustainable synthesis methods for compounds like this one are gaining traction, highlighting the importance of environmentally friendly production processes.

In conclusion, 1-Methyl-4-(phenylsulfamoyl)-1H-pyrrole-2-carboxamide (CAS No. 1000932-96-6) represents a fascinating area of study with broad implications for pharmaceutical research and drug development. Its unique chemical structure and potential biological activities position it as a valuable tool for scientists exploring new avenues in bioactive molecule design. As research progresses, this compound may unlock new possibilities for treating various health conditions, underscoring the importance of continued investigation into its properties and applications.

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