Cas no 17011-53-9 (1,3-Isobenzofurandione, 5-amino-)

1,3-Isobenzofurandione, 5-amino- structure
17011-53-9 structure
Product Name:1,3-Isobenzofurandione, 5-amino-
CAS No:17011-53-9
MF:C8H5NO3
MW:163.130202054977
MDL:MFCD00127683
CID:96292
PubChem ID:13814390
Update Time:2025-04-24

1,3-Isobenzofurandione, 5-amino- Chemical and Physical Properties

Names and Identifiers

    • 1,3-Isobenzofurandione, 5-amino-
    • 5-amino-2-benzofuran-1,3-dione
    • YJDUJNZZWJMRJT-UHFFFAOYSA-N
    • DTXSID60550354
    • MFCD00127683
    • AKOS006275171
    • 4-aminophthalic anhydride
    • CS-0370543
    • 5-aminoisobenzofuran-1,3-dione
    • 17011-53-9
    • SCHEMBL4547348
    • G72711
    • MDL: MFCD00127683
    • Inchi: 1S/C8H5NO3/c9-4-1-2-5-6(3-4)8(11)12-7(5)10/h1-3H,9H2
    • InChI Key: YJDUJNZZWJMRJT-UHFFFAOYSA-N
    • SMILES: O1C(C2C=CC(=CC=2C1=O)N)=O

Computed Properties

  • Exact Mass: 163.02695
  • Monoisotopic Mass: 163.026943022g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 0
  • Complexity: 239
  • 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
  • Topological Polar Surface Area: 69.4?2

Experimental Properties

  • PSA: 69.39

1,3-Isobenzofurandione, 5-amino- Pricemore >>

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1,3-Isobenzofurandione, 5-amino- Suppliers

Amadis Chemical Company Limited
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(CAS:17011-53-9)1,3-Isobenzofurandione, 5-amino-
Order Number:A1002504
Stock Status:in Stock
Quantity:250mg/1g/5g/10g/25g
Purity:99%
Pricing Information Last Updated:Thursday, 29 August 2024 14:59
Price ($):206.0/403.0/634.0/1070.0/2247.0

1,3-Isobenzofurandione, 5-amino- Related Literature

Additional information on 1,3-Isobenzofurandione, 5-amino-

5-Amino-1,3-Isobenzofurandione: Properties, Applications, and Market Insights

5-Amino-1,3-Isobenzofurandione (CAS No. 17011-53-9) is a specialized organic compound with significant applications in pharmaceuticals, agrochemicals, and material science. This heterocyclic derivative of isobenzofuran-1,3-dione is gaining attention due to its unique chemical properties and versatility in synthesis. Researchers and industries are increasingly exploring its potential, especially in the development of novel bioactive molecules and advanced materials.

The molecular structure of 5-amino-1,3-isobenzofurandione features an amino group attached to the aromatic ring, enhancing its reactivity and making it a valuable intermediate in organic synthesis. Its chemical formula is C8H5NO3, and it exhibits a molecular weight of 163.13 g/mol. The compound is typically a crystalline solid with moderate solubility in polar organic solvents, which facilitates its use in various chemical reactions.

One of the key applications of 5-amino-1,3-isobenzofurandione is in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). Its structural motif is found in several drug candidates targeting inflammatory diseases and metabolic disorders. Recent studies have highlighted its role in the development of small-molecule inhibitors, which are crucial in modern drug discovery.

In agrochemicals, 5-amino-1,3-isobenzofurandione derivatives are being investigated for their potential as plant growth regulators and pesticide intermediates. The compound's ability to interact with biological systems makes it a promising candidate for sustainable agricultural solutions. With the growing demand for eco-friendly agrochemicals, this compound is expected to play a significant role in future formulations.

The material science field also benefits from 5-amino-1,3-isobenzofurandione, particularly in the development of high-performance polymers and functional coatings. Its incorporation into polymer chains can enhance thermal stability and mechanical properties, making it suitable for aerospace, automotive, and electronics applications. Researchers are exploring its use in photoactive materials for solar cells and optoelectronic devices.

Market trends indicate a rising demand for 5-amino-1,3-isobenzofurandione, driven by advancements in pharmaceutical and material science research. The compound's global market is projected to grow steadily, with key players investing in scalable synthesis methods to meet industrial needs. Innovations in green chemistry are also influencing production processes, reducing environmental impact while maintaining high yields.

For researchers and manufacturers, understanding the synthesis pathways of 5-amino-1,3-isobenzofurandione is critical. Common methods include the amination of phthalic anhydride derivatives or the oxidation of amino-substituted precursors. Optimizing these processes for cost-efficiency and sustainability remains a focus area in chemical engineering.

Safety and handling of 5-amino-1,3-isobenzofurandione require standard laboratory precautions, including the use of personal protective equipment (PPE) and proper ventilation. While not classified as hazardous under normal conditions, it is essential to follow chemical safety guidelines to prevent exposure and ensure safe storage.

In conclusion, 5-amino-1,3-isobenzofurandione (CAS No. 17011-53-9) is a multifaceted compound with broad applications across industries. Its unique properties and growing market demand underscore its importance in modern chemistry. As research continues to uncover new uses, this compound is poised to become a cornerstone in the development of innovative solutions for healthcare, agriculture, and technology.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:17011-53-9)1,3-Isobenzofurandione, 5-amino-
A1002504
Purity:99%/99%/99%/99%/99%
Quantity:250mg/1g/5g/10g/25g
Price ($):206.0/403.0/634.0/1070.0/2247.0
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