Cas no 51012-30-7 (2-(4-fluorobenzenesulfonamido)benzoic acid)

2-(4-Fluorobenzenesulfonamido)benzoic acid is a sulfonamide-derived benzoic acid compound featuring a fluorinated aromatic ring. Its molecular structure combines a sulfonamide linker with a carboxylic acid functional group, making it a versatile intermediate in organic synthesis and pharmaceutical research. The presence of the fluorine atom enhances its electronic properties, potentially improving binding affinity in medicinal chemistry applications. This compound is particularly useful in the development of enzyme inhibitors or as a precursor for more complex sulfonamide-based molecules. Its well-defined structure and reactivity profile allow for precise modifications, supporting its use in targeted drug discovery and biochemical studies.
2-(4-fluorobenzenesulfonamido)benzoic acid structure
51012-30-7 structure
Product Name:2-(4-fluorobenzenesulfonamido)benzoic acid
CAS No:51012-30-7
MF:C13H10FNO4S
MW:295.286205768585
MDL:MFCD00114880
CID:370062
PubChem ID:39853
Update Time:2025-05-21

2-(4-fluorobenzenesulfonamido)benzoic acid Chemical and Physical Properties

Names and Identifiers

    • Benzoic acid,2-[[(4-fluorophenyl)sulfonyl]amino]-
    • 2-(4-Fluoro-benzenesulfonylamino)-benzoic acid
    • 2-(((4-fluorophenyl)sulfonyl)amino)-benzoicaci
    • 2-[(4-fluorophenyl)sulfonylamino]benzoic acid
    • 2-{[(4-Fluorophenyl)sulfonyl]amino}benzoic acid
    • 2-(4-fluorobenzenesulfonamido)benzoic acid
    • 2-(4-Fluorophenylsulfonamido)benzoicacid
    • BRN 2390363
    • 51012-30-7
    • F2124-0508
    • AKOS000114689
    • DTXSID90199018
    • Z45511843
    • BENZOIC ACID, 2-(((4-FLUOROPHENYL)SULFONYL)AMINO)-
    • 2-(((4-Fluorophenyl)sulfonyl)amino)benzoic acid
    • CHEMBL3250338
    • 2-(4-Fluorophenylsulfonamido)benzoic acid
    • MFCD00114880
    • EN300-00319
    • SB82596
    • MDL: MFCD00114880
    • Inchi: 1S/C13H10FNO4S/c14-9-5-7-10(8-6-9)20(18,19)15-12-4-2-1-3-11(12)13(16)17/h1-8,15H,(H,16,17)
    • InChI Key: YPVRMONLTQLVQE-UHFFFAOYSA-N
    • SMILES: S(C1C=CC(=CC=1)F)(NC1C=CC=CC=1C(=O)O)(=O)=O

Computed Properties

  • Exact Mass: 295.0315
  • Monoisotopic Mass: 295.031457
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 20
  • Rotatable Bond Count: 4
  • Complexity: 440
  • 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: 2.2
  • Topological Polar Surface Area: 91.8

Experimental Properties

  • Density: 1.512
  • Boiling Point: 472.4°Cat760mmHg
  • Flash Point: 239.5°C
  • Refractive Index: 1.639
  • PSA: 83.47

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2-(4-fluorobenzenesulfonamido)benzoic acid Suppliers

Amadis Chemical Company Limited
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Audited Supplier Audited Supplier
(CAS:51012-30-7)2-(4-fluorobenzenesulfonamido)benzoic acid
Order Number:A1164112
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 00:20
Price ($):300.0

Additional information on 2-(4-fluorobenzenesulfonamido)benzoic acid

Recent Advances in the Study of 2-(4-Fluorobenzenesulfonamido)benzoic Acid (CAS: 51012-30-7)

The compound 2-(4-fluorobenzenesulfonamido)benzoic acid (CAS: 51012-30-7) has recently garnered significant attention in the field of chemical biology and pharmaceutical research. This sulfonamide derivative, characterized by its unique structural features, has shown promising potential in various therapeutic applications. Recent studies have focused on its synthesis, mechanism of action, and biological activities, particularly in the context of anti-inflammatory and anticancer properties. This research brief aims to summarize the latest findings and highlight the compound's potential as a lead molecule for drug development.

One of the key areas of investigation has been the synthesis and optimization of 2-(4-fluorobenzenesulfonamido)benzoic acid. Researchers have developed novel synthetic routes to improve yield and purity, which are critical for its pharmaceutical applications. Advanced techniques such as high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy have been employed to characterize the compound and ensure its structural integrity. These efforts have paved the way for more detailed pharmacological studies.

In terms of biological activity, recent studies have demonstrated that 2-(4-fluorobenzenesulfonamido)benzoic acid exhibits potent anti-inflammatory effects by inhibiting key enzymes involved in the inflammatory cascade, such as cyclooxygenase-2 (COX-2). This mechanism is similar to that of nonsteroidal anti-inflammatory drugs (NSAIDs), but with potentially fewer side effects due to its selective inhibition. Additionally, the compound has shown promising results in preclinical models of cancer, where it has been found to induce apoptosis in certain cancer cell lines, suggesting its potential as an anticancer agent.

Another significant aspect of the research has been the exploration of the compound's pharmacokinetic properties. Studies have investigated its absorption, distribution, metabolism, and excretion (ADME) profiles to better understand its behavior in biological systems. These findings are crucial for the development of formulations that can enhance its bioavailability and therapeutic efficacy. Preliminary data indicate that 2-(4-fluorobenzenesulfonamido)benzoic acid has favorable pharmacokinetic characteristics, making it a viable candidate for further development.

Despite these promising findings, challenges remain in the clinical translation of 2-(4-fluorobenzenesulfonamido)benzoic acid. Issues such as solubility, stability, and potential toxicity need to be addressed through further research. However, the compound's unique structural and functional properties make it a compelling subject for ongoing studies. Future research directions may include the development of derivatives with enhanced activity and reduced side effects, as well as the exploration of its potential in combination therapies.

In conclusion, 2-(4-fluorobenzenesulfonamido)benzoic acid (CAS: 51012-30-7) represents a promising molecule in the field of chemical biology and pharmaceutical research. Its demonstrated anti-inflammatory and anticancer activities, coupled with favorable pharmacokinetic properties, highlight its potential as a lead compound for drug development. Continued research efforts will be essential to fully realize its therapeutic potential and address the remaining challenges in its clinical application.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:51012-30-7)2-(4-fluorobenzenesulfonamido)benzoic acid
A1164112
Purity:99%
Quantity:1g
Price ($):300.0
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