Cas no 1039993-93-5 (2,6-difluoro-3-(methylsulfamoyl)benzoic acid)

2,6-Difluoro-3-(methylsulfamoyl)benzoic acid is a fluorinated benzoic acid derivative featuring a methylsulfamoyl substituent at the 3-position. This compound is of interest in pharmaceutical and agrochemical research due to its potential as a versatile intermediate in the synthesis of biologically active molecules. The presence of fluorine atoms enhances metabolic stability and bioavailability, while the methylsulfamoyl group contributes to selective binding interactions. Its well-defined structure and high purity make it suitable for use in medicinal chemistry, particularly in the development of enzyme inhibitors or receptor modulators. The compound’s reactivity allows for further functionalization, enabling tailored modifications for targeted applications.
2,6-difluoro-3-(methylsulfamoyl)benzoic acid structure
1039993-93-5 structure
Product Name:2,6-difluoro-3-(methylsulfamoyl)benzoic acid
CAS No:1039993-93-5
MF:C8H7F2NO4S
MW:251.20728802681
CID:4569196
PubChem ID:29286499
Update Time:2025-05-20

2,6-difluoro-3-(methylsulfamoyl)benzoic acid Chemical and Physical Properties

Names and Identifiers

    • Benzoic acid, 2,6-difluoro-3-[(methylamino)sulfonyl]-
    • 2,6-Difluoro-3-(methylsulfamoyl)benzoic Acid
    • 2,6-difluoro-3-(methylsulfamoyl)benzoic acid
    • Inchi: 1S/C8H7F2NO4S/c1-11-16(14,15)5-3-2-4(9)6(7(5)10)8(12)13/h2-3,11H,1H3,(H,12,13)
    • InChI Key: XEJQTMPTFBEQLE-UHFFFAOYSA-N
    • SMILES: C(O)(=O)C1=C(F)C=CC(S(NC)(=O)=O)=C1F

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Additional information on 2,6-difluoro-3-(methylsulfamoyl)benzoic acid

Comprehensive Overview of 2,6-Difluoro-3-(methylsulfamoyl)benzoic acid (CAS No. 1039993-93-5)

2,6-Difluoro-3-(methylsulfamoyl)benzoic acid (CAS No. 1039993-93-5) is a fluorinated benzoic acid derivative with significant applications in pharmaceutical and agrochemical research. This compound, characterized by its sulfamoyl and carboxylic acid functional groups, has garnered attention for its potential as a building block in drug discovery. Researchers are increasingly exploring its utility in designing enzyme inhibitors and bioactive molecules, particularly in targeting inflammatory pathways and metabolic disorders.

The structural uniqueness of 2,6-difluoro-3-(methylsulfamoyl)benzoic acid lies in its difluorinated aromatic ring, which enhances metabolic stability and bioavailability—a critical factor in modern medicinal chemistry. Recent studies highlight its role in optimizing lead compounds for diseases like diabetes and autoimmune conditions, aligning with the growing demand for precision medicine solutions. Its CAS No. 1039993-93-5 is frequently cited in patent literature, underscoring its industrial relevance.

From a synthetic perspective, this compound serves as a versatile intermediate for cross-coupling reactions and amide bond formation. Its compatibility with green chemistry principles—such as reduced solvent waste—resonates with the pharmaceutical industry's shift toward sustainable practices. Analysts note rising interest in fluorinated sulfonamides, driven by their improved pharmacokinetic profiles, placing 1039993-93-5 at the forefront of innovation.

Beyond pharmaceuticals, 2,6-difluoro-3-(methylsulfamoyl)benzoic acid finds niche applications in material science, particularly in designing high-performance polymers with enhanced thermal resistance. Its electron-withdrawing properties make it valuable for tuning electronic materials, a topic gaining traction in organic electronics research. Regulatory agencies classify it as non-hazardous under standard handling conditions, facilitating its adoption in diverse R&D settings.

In summary, CAS No. 1039993-93-5 represents a multifaceted tool for researchers addressing challenges in drug development and advanced materials. Its combination of fluorine and sulfonamide moieties offers a strategic advantage in molecular design, reflecting broader trends toward structure-activity relationship optimization. As the scientific community prioritizes small-molecule therapeutics, this compound’s role is poised to expand, supported by robust synthetic protocols and safety profiles.

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