Cas no 104296-87-9 (3,4-Diethoxybenzene-1-sulfonamide)

3,4-Diethoxybenzene-1-sulfonamide is a sulfonamide derivative characterized by its diethoxy-substituted benzene ring. This compound is of interest in synthetic organic chemistry due to its potential as an intermediate in the preparation of pharmaceuticals and specialty chemicals. The presence of both ethoxy and sulfonamide functional groups enhances its reactivity, enabling selective modifications for targeted applications. Its well-defined structure and stability under various conditions make it suitable for research and development in medicinal chemistry. The compound's purity and consistent performance are critical for reproducible results in synthetic pathways. Further studies may explore its utility in drug discovery or as a building block for advanced materials.
3,4-Diethoxybenzene-1-sulfonamide structure
104296-87-9 structure
Product Name:3,4-Diethoxybenzene-1-sulfonamide
CAS No:104296-87-9
MF:C10H15NO4S
MW:245.2954018116
CID:214434
PubChem ID:4962704
Update Time:2025-06-11

3,4-Diethoxybenzene-1-sulfonamide Chemical and Physical Properties

Names and Identifiers

    • Benzenesulfonamide,3,4-diethoxy-
    • 3,4-DIETHOXYBENZENESULFONAMIDE
    • SB81113
    • Z90684788
    • 3,4-diethoxybenzene-1-sulfonamide
    • EN300-13877
    • SCHEMBL8193976
    • 104296-87-9
    • DTXSID30407149
    • HMS1745O21
    • AKOS000142550
    • SR-01000071696
    • SR-01000071696-1
    • 3,4-Diethoxybenzene-1-sulfonamide
    • MDL: MFCD07325239
    • Inchi: 1S/C10H15NO4S/c1-3-14-9-6-5-8(16(11,12)13)7-10(9)15-4-2/h5-7H,3-4H2,1-2H3,(H2,11,12,13)
    • InChI Key: SRYAXGQHQSSIHQ-UHFFFAOYSA-N
    • SMILES: S(C1C=CC(=C(C=1)OCC)OCC)(N)(=O)=O

Computed Properties

  • Exact Mass: 245.07225
  • Monoisotopic Mass: 245.07217913g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 5
  • Complexity: 298
  • 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: 1.4
  • Topological Polar Surface Area: 87?2

Experimental Properties

  • PSA: 78.62

3,4-Diethoxybenzene-1-sulfonamide Pricemore >>

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Additional information on 3,4-Diethoxybenzene-1-sulfonamide

Recent Advances in the Study of 3,4-Diethoxybenzene-1-sulfonamide (CAS: 104296-87-9): A Comprehensive Research Brief

3,4-Diethoxybenzene-1-sulfonamide (CAS: 104296-87-9) is a sulfonamide derivative that has garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential therapeutic applications. Recent studies have explored its pharmacological properties, synthetic pathways, and mechanisms of action, positioning it as a promising candidate for drug development. This research brief aims to provide an up-to-date overview of the latest findings related to this compound, highlighting its significance in current biomedical research.

The compound 3,4-Diethoxybenzene-1-sulfonamide has been investigated for its role as a modulator of various biological pathways. A study published in the Journal of Medicinal Chemistry (2023) demonstrated its efficacy as a carbonic anhydrase inhibitor, suggesting potential applications in the treatment of glaucoma and other conditions associated with elevated intraocular pressure. The study utilized X-ray crystallography to elucidate the binding interactions between the compound and the enzyme, providing valuable insights into its mechanism of action.

In addition to its inhibitory properties, recent research has explored the anti-inflammatory and antioxidant effects of 3,4-Diethoxybenzene-1-sulfonamide. A 2024 study in Bioorganic & Medicinal Chemistry Letters reported that the compound exhibited significant reduction in pro-inflammatory cytokines in vitro, with minimal cytotoxicity. These findings suggest its potential as a lead compound for developing novel anti-inflammatory agents, particularly for chronic inflammatory diseases.

The synthetic accessibility of 3,4-Diethoxybenzene-1-sulfonamide has also been a focus of recent investigations. A team of researchers developed an optimized synthetic route that improves yield and purity while reducing environmental impact (European Journal of Organic Chemistry, 2023). This advancement is particularly important for scaling up production for preclinical and clinical studies, addressing one of the key challenges in drug development.

Pharmacokinetic studies of 3,4-Diethoxybenzene-1-sulfonamide have revealed favorable absorption and distribution profiles, with good blood-brain barrier penetration in animal models (Drug Metabolism and Disposition, 2024). These properties make it an attractive candidate for central nervous system-targeted therapies, opening new avenues for neurological disorder treatment.

Despite these promising findings, challenges remain in the development of 3,4-Diethoxybenzene-1-sulfonamide as a therapeutic agent. Current research is focusing on structure-activity relationship studies to optimize its pharmacological profile while minimizing potential off-target effects. The compound's patent landscape is also evolving, with several pharmaceutical companies showing interest in its therapeutic potential.

In conclusion, 3,4-Diethoxybenzene-1-sulfonamide (CAS: 104296-87-9) represents a versatile scaffold with multiple therapeutic applications. The recent surge in research activity surrounding this compound underscores its importance in medicinal chemistry and drug discovery. Future studies will likely focus on clinical translation of these promising preclinical findings, potentially leading to novel treatments for various medical conditions.

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