Cas no 6357-85-3 (3-hydroxynaphthalene-1-sulfonic Acid)

3-Hydroxynaphthalene-1-sulfonic acid is a versatile intermediate in organic synthesis, primarily used in the production of dyes, pigments, and pharmaceuticals. Its sulfonic acid and hydroxyl functional groups enable efficient coupling reactions, making it valuable for azo dye manufacturing. The compound exhibits good solubility in water and polar solvents, facilitating its use in aqueous reaction systems. Its stability under moderate conditions ensures reliable performance in industrial applications. Additionally, it serves as a key precursor for synthesizing naphthalene-based derivatives with tailored properties. The product is characterized by high purity and consistent quality, meeting stringent requirements for specialized chemical processes.
3-hydroxynaphthalene-1-sulfonic Acid structure
6357-85-3 structure
Product Name:3-hydroxynaphthalene-1-sulfonic Acid
CAS No:6357-85-3
MF:C10H8O4S
MW:224.233121871948
MDL:MFCD19302726
CID:507134
Update Time:2026-04-29

3-hydroxynaphthalene-1-sulfonic Acid Chemical and Physical Properties

Names and Identifiers

    • 1-Naphthalenesulfonicacid, 3-hydroxy-
    • 3-hydroxy-1-Naphthalenesulfonicacid
    • 3-hydroxynaphthalenesulphonic acid
    • 3-hydroxynaphthalene-1-sulfonic acid
    • methyl 4-(5-{(E)-[1-(3-bromophenyl)-2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene]methyl}furan-2-yl)benzoate
    • 3-hydroxynaphthalene-1-sulfonic Acid
    • MDL: MFCD19302726

Computed Properties

  • Exact Mass: 224.01434

Experimental Properties

  • PSA: 74.6

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Additional information on 3-hydroxynaphthalene-1-sulfonic Acid

Introduction to 3-hydroxynaphthalene-1-sulfonic Acid (CAS No: 6357-85-3)

3-hydroxynaphthalene-1-sulfonic Acid, identified by the Chemical Abstracts Service registry number CAS No: 6357-85-3, is a significant organic compound widely utilized in pharmaceutical synthesis, chemical research, and industrial applications. This compound belongs to the class of naphthalene derivatives, characterized by the presence of both hydroxyl and sulfonic acid functional groups. Its unique structural properties make it a valuable intermediate in the development of various chemical products, particularly in the pharmaceutical sector.

The molecular structure of 3-hydroxynaphthalene-1-sulfonic Acid consists of a naphthalene ring system substituted with a hydroxyl group at the 3-position and a sulfonic acid group at the 1-position. This arrangement imparts distinct reactivity and solubility characteristics, making it highly useful in organic synthesis. The sulfonic acid group enhances its solubility in polar solvents, while the hydroxyl group allows for further functionalization through various chemical reactions such as esterification, etherification, and condensation reactions.

In recent years, 3-hydroxynaphthalene-1-sulfonic Acid has garnered attention in the field of medicinal chemistry due to its potential applications in drug development. Researchers have explored its role as a precursor in synthesizing complex pharmaceutical molecules. For instance, it has been investigated as a building block for designing novel anti-inflammatory agents and analgesics. The presence of both hydroxyl and sulfonic acid functionalities provides multiple sites for chemical modification, enabling the creation of derivatives with tailored biological activities.

One of the most compelling aspects of 3-hydroxynaphthalene-1-sulfonic Acid is its versatility in synthetic chemistry. It serves as a key intermediate in the preparation of sulfonamides, which are known for their broad spectrum of biological activities. Sulfonamides are widely used in antibiotics, diuretics, and other therapeutic agents. The ability to functionalize 3-hydroxynaphthalene-1-sulfonic Acid allows chemists to design molecules that interact specifically with biological targets, enhancing drug efficacy and reducing side effects.

Recent studies have also highlighted the compound's role in material science. The unique properties of 3-hydroxynaphthalene-1-sulfonic Acid, such as its ability to form stable complexes with metals and its compatibility with various polymers, make it suitable for use in advanced materials. For example, it has been explored as a component in conductive polymers and metal-organic frameworks (MOFs). These materials have potential applications in electronics, catalysis, and gas storage.

The industrial production of 3-hydroxynaphthalene-1-sulfonic Acid typically involves sulfonation followed by hydroxylation of naphthalene derivatives. Advances in green chemistry have led to the development of more sustainable synthetic routes, minimizing waste and reducing environmental impact. These processes often employ catalytic methods that improve yield and selectivity while maintaining cost-effectiveness.

In academic research, 3-hydroxynaphthalene-1-sulfonic Acid continues to be a subject of investigation due to its reactivity and structural diversity. Researchers are exploring new synthetic pathways to access novel derivatives with enhanced properties. For instance, palladium-catalyzed cross-coupling reactions have been employed to introduce additional functional groups onto the naphthalene core, expanding its utility in drug discovery.

The pharmaceutical industry has shown particular interest in 3-hydroxynaphthalene-1-sulfonic Acid as a scaffold for developing new therapeutics. Its structural features allow for the creation of molecules that can modulate various biological pathways. Ongoing clinical trials are evaluating derivatives of this compound for their potential in treating conditions such as cancer, inflammation, and infectious diseases. The results from these trials could lead to significant advancements in patient care.

Beyond pharmaceuticals, 3-hydroxynaphthalene-1-sulfonic Acid finds applications in other industries as well. In dye manufacturing, it serves as an intermediate for producing vibrant pigments used in textiles and coatings. Its ability to form stable complexes with metal ions also makes it valuable in water treatment processes, where it helps remove heavy metals from wastewater through ion exchange mechanisms.

The future prospects for 3-hydroxynaphthalene-1-sulfonic Acid are promising, driven by ongoing research and technological advancements. As synthetic methodologies continue to evolve, new applications for this compound are likely to emerge. Collaborative efforts between academia and industry will be crucial in translating laboratory discoveries into practical solutions that benefit society.

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