Cas no 41704-95-4 (2,3-Dioxoindoline-4-carboxylic acid)

2,3-Dioxoindoline-4-carboxylic acid is a versatile heterocyclic compound featuring both a carboxylic acid and a dioxoindoline moiety, making it a valuable intermediate in organic synthesis and pharmaceutical research. Its structure allows for diverse functionalization, enabling applications in the development of bioactive molecules, including potential therapeutic agents. The compound’s reactivity is particularly useful in constructing indole-based scaffolds, which are prevalent in medicinal chemistry. High purity and stability under standard conditions ensure consistent performance in synthetic workflows. Its compatibility with a range of coupling and condensation reactions further enhances its utility as a building block for complex molecular architectures.
2,3-Dioxoindoline-4-carboxylic acid structure
41704-95-4 structure
Product Name:2,3-Dioxoindoline-4-carboxylic acid
CAS No:41704-95-4
MF:C9H5NO4
MW:191.140302419662
MDL:MFCD16876980
CID:1094866
PubChem ID:23298204
Update Time:2025-11-02

2,3-Dioxoindoline-4-carboxylic acid Chemical and Physical Properties

Names and Identifiers

    • 2,3-Dioxoindoline-4-carboxylic acid
    • 2,3-dioxo-1H-indole-4-carboxylic acid
    • 1H-Indole-4-carboxylic acid, 2,3-dihydro-2,3-dioxo-
    • FCH1178521
    • AK149923
    • AX8287148
    • 2,3-Dihydro-2,3-dioxo-1H-indole-4-carboxylic acid
    • 2,3-Dioxo-2,3-dihydro-1H-indole-4-carboxylic acid
    • CS-0093860
    • SB66135
    • DB-022964
    • AS-62157
    • DTXSID80632686
    • SCHEMBL4625089
    • MFCD16876980
    • 2,3-Dioxoindoline-4-carboxylicacid
    • A918442
    • C75115
    • AKOS015855803
    • isatin-4-carboxylic acid
    • 41704-95-4
    • MDL: MFCD16876980
    • Inchi: 1S/C9H5NO4/c11-7-6-4(9(13)14)2-1-3-5(6)10-8(7)12/h1-3H,(H,13,14)(H,10,11,12)
    • InChI Key: ZTBVJLXMEWWFHD-UHFFFAOYSA-N
    • SMILES: O=C1C(NC2C=CC=C(C(=O)O)C=21)=O

Computed Properties

  • Exact Mass: 191.02185764g/mol
  • Monoisotopic Mass: 191.02185764g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 312
  • 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: 0.2
  • Topological Polar Surface Area: 83.5

Experimental Properties

  • Density: 1.6±0.1 g/cm3

2,3-Dioxoindoline-4-carboxylic acid Security Information

2,3-Dioxoindoline-4-carboxylic acid Pricemore >>

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Additional information on 2,3-Dioxoindoline-4-carboxylic acid

Exploring the Versatile Applications and Properties of 2,3-Dioxoindoline-4-carboxylic acid (CAS No. 41704-95-4)

2,3-Dioxoindoline-4-carboxylic acid (CAS No. 41704-95-4) is a highly specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, characterized by its unique indoline-4-carboxylic acid structure, serves as a critical intermediate in the synthesis of various bioactive molecules. Researchers and industry professionals are increasingly interested in its potential applications, particularly in drug discovery and development.

The molecular structure of 2,3-Dioxoindoline-4-carboxylic acid features a fused bicyclic system with two carbonyl groups at positions 2 and 3, and a carboxylic acid moiety at position 4. This arrangement imparts distinct chemical properties, making it a valuable building block in organic synthesis. Recent studies highlight its role in creating novel heterocyclic compounds, which are pivotal in designing new therapeutic agents.

One of the most compelling aspects of 2,3-Dioxoindoline-4-carboxylic acid is its utility in medicinal chemistry. The compound's ability to undergo various chemical transformations allows for the creation of derivatives with potential pharmacological activities. For instance, it has been explored in the development of anti-inflammatory agents and antioxidant compounds, addressing some of the most pressing health concerns today.

In addition to its pharmaceutical applications, 2,3-Dioxoindoline-4-carboxylic acid is also investigated for its role in material science. Its unique structural features make it a candidate for developing advanced organic electronic materials, which are essential for next-generation devices like flexible displays and solar cells. This dual applicability in both life sciences and material sciences underscores its versatility.

The synthesis of 2,3-Dioxoindoline-4-carboxylic acid typically involves multi-step organic reactions, starting from readily available precursors. Researchers have optimized these processes to improve yield and purity, ensuring that the compound meets the stringent requirements of industrial and academic applications. Recent advancements in green chemistry have also led to more sustainable synthesis routes, aligning with global efforts to reduce environmental impact.

Market trends indicate a growing demand for 2,3-Dioxoindoline-4-carboxylic acid, driven by its expanding applications in drug discovery and material science. Pharmaceutical companies and research institutions are actively seeking high-quality supplies of this compound to support their R&D efforts. As a result, manufacturers are scaling up production while maintaining strict quality control measures to meet industry standards.

For those looking to purchase 2,3-Dioxoindoline-4-carboxylic acid, it is essential to source it from reputable suppliers who provide detailed analytical data, including HPLC purity and spectroscopic characterization. This ensures the compound's suitability for sensitive applications, such as high-throughput screening and structure-activity relationship studies.

In conclusion, 2,3-Dioxoindoline-4-carboxylic acid (CAS No. 41704-95-4) stands out as a multifaceted compound with significant potential across various scientific disciplines. Its unique chemical properties, coupled with its broad applicability, make it a valuable asset in both research and industrial settings. As advancements in synthetic methodologies and application areas continue to emerge, the importance of this compound is expected to grow even further.

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