Cas no 365549-33-3 (5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid)

5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid is a polycarboxylic acid derivative featuring a diazenyl linker between two benzene rings, each substituted with carboxyl groups. This structure imparts strong chelating properties, making it suitable for applications in coordination chemistry and metal-organic framework (MOF) synthesis. Its multiple carboxylate groups enable robust binding to metal ions, facilitating the formation of stable complexes. The compound’s aromatic backbone and azo linkage contribute to its potential use in dye chemistry or as a functional linker in advanced materials. Its high solubility in polar solvents further enhances its utility in solution-phase reactions. This product is valued for its versatility in designing tailored molecular architectures.
5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid structure
365549-33-3 structure
Product Name:5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid
CAS No:365549-33-3
MF:C16H10N2O8
MW:358.259204387665
MDL:MFCD30738344
CID:2950460
PubChem ID:15526883
Update Time:2025-10-28

5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid Chemical and Physical Properties

Names and Identifiers

    • (E)-5,5'-(diazene-1,2-diyl)diisophthalic acid
    • 5,5'-Azobisisophthalic acid
    • 9528AF
    • 5,5'-[(E)-Diazene-1,2-diyl]bisisophthalic acid
    • 3,3',5,5'-Azobenzene tetracarboxylic acid, TazbH4
    • 3,3',5,5'-Azobenzene tetracarboxylic acid
    • 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid
    • YSZC029
    • SCHEMBL842276
    • 5,5'-(diazene-1,2-diyl)diisophthalic acid
    • azObenzene tetracarboxylic acid
    • AT25834
    • 365549-33-3
    • DTXSID201191597
    • (E)-5,5'-(diazene-1,2-diyl)diisophthalicacid
    • 1,3-Benzenedicarboxylic acid, 5,5'-(1,2-diazenediyl)bis- ;(e)-5,5'-(diazene-1,2-diyl)diisophthalic acid
    • MFCD30738344
    • Bis(3,5-dicarboxyphenyl)azo
    • BS-45922
    • CS-0107505
    • 5,5a(2)-(1E)-1,2-Diazenediylbis[1,3-benzenedicarboxylic acid]
    • 1007597-56-9
    • 5-[2-(3,5-dicarboxyphenyl)diazen-1-yl]benzene-1,3-dicarboxylic acid
    • 1,3-Benzenedicarboxylic acid, 5,5'-(1E)-1,2-diazenediylbis-
    • MDL: MFCD30738344
    • Inchi: 1S/C16H10N2O8/c19-13(20)7-1-8(14(21)22)4-11(3-7)17-18-12-5-9(15(23)24)2-10(6-12)16(25)26/h1-6H,(H,19,20)(H,21,22)(H,23,24)(H,25,26)/b18-17+
    • InChI Key: MXBBZODCMBYDCL-ISLYRVAYSA-N
    • SMILES: OC(C1C=C(C(=O)O)C=C(C=1)/N=N/C1C=C(C(=O)O)C=C(C(=O)O)C=1)=O

Computed Properties

  • Exact Mass: 358.04371528g/mol
  • Monoisotopic Mass: 358.04371528g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 10
  • Heavy Atom Count: 26
  • Rotatable Bond Count: 6
  • Complexity: 523
  • 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
  • Topological Polar Surface Area: 174
  • XLogP3: 1.8

Experimental Properties

  • Color/Form: No data avaiable
  • Density: 1.2±0.1 g/cm3
  • Melting Point: No data available
  • Boiling Point: 432.4±45.0 °C at 760 mmHg
  • Flash Point: 215.3±28.7 °C
  • Stability/Shelf Life: store cold
  • Vapor Pressure: No data available

5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid Security Information

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5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid Suppliers

Suzhou Senfeida Chemical Co., Ltd
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(CAS:365549-33-3)(E)-5,5'-(diazene-1,2-diyl)diisophthalic acid
Order Number:sfd5202
Stock Status:in Stock
Quantity:200kg
Purity:99.9%
Pricing Information Last Updated:Friday, 19 July 2024 14:33
Price ($):discuss personally

Additional information on 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid

Comprehensive Overview of 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid (CAS No. 365549-33-3)

5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid (CAS No. 365549-33-3) is a highly specialized organic compound belonging to the class of azo-linked polycarboxylic acids. This compound has garnered significant attention in recent years due to its unique structural properties and potential applications in advanced materials science, particularly in the fields of coordination polymers, metal-organic frameworks (MOFs), and dye-sensitized solar cells (DSSCs). The presence of multiple carboxylic acid groups and an azo linkage in its molecular structure makes it a versatile building block for designing functional materials with tailored properties.

The compound's systematic name, 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid, reflects its precise chemical architecture, which consists of two benzene rings connected by an azo group (-N=N-) and decorated with carboxylic acid (-COOH) substituents. This arrangement not only enhances its ability to form strong coordination bonds with metal ions but also contributes to its solubility in polar solvents, making it suitable for various solution-phase synthesis applications. Researchers have explored its use in creating porous materials for gas storage, catalysis, and even drug delivery systems, aligning with current trends in sustainable chemistry and green technology.

In the context of renewable energy, 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid has shown promise as a photoactive component in DSSCs. Its ability to absorb visible light and transfer electrons efficiently makes it a candidate for improving the performance of next-generation solar cells. This aligns with the growing global demand for clean energy solutions and the increasing interest in organic photovoltaics. Additionally, its chromophoric properties have sparked investigations into its potential as a molecular sensor for detecting environmental pollutants, a topic of high relevance in today's environmental monitoring discussions.

From a synthetic chemistry perspective, the compound's multidentate ligand capability allows for the construction of intricate supramolecular architectures. This has led to its use in developing luminescent materials for OLEDs and other optoelectronic devices, addressing the need for more efficient display technologies. The aza-coupling reaction used in its synthesis is also a subject of interest for researchers working on click chemistry and modular synthesis approaches, which are currently trending in drug discovery and material science communities.

Quality control and characterization of 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid typically involve advanced analytical techniques such as HPLC, NMR spectroscopy, and mass spectrometry. These methods ensure the compound's purity and confirm its structural integrity, which is crucial for its performance in high-value applications. The compound's thermal stability and solubility profile have also been extensively studied, as these properties determine its suitability for specific industrial processes.

As research continues to explore the frontiers of functional materials, 5-[(3,5-Dicarboxyphenyl)diazenyl]benzene-1,3-dicarboxylic acid remains at the forefront of innovation. Its combination of structural versatility and functional diversity positions it as a key player in addressing contemporary challenges in energy storage, environmental remediation, and advanced manufacturing. With the increasing emphasis on molecular engineering and smart materials, this compound is likely to see expanded applications in emerging technologies in the coming years.

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Suzhou Senfeida Chemical Co., Ltd
(CAS:365549-33-3)(E)-5,5'-(diazene-1,2-diyl)diisophthalic acid
sfd5202
Purity:99.9%
Quantity:200kg
Price ($):Inquiry
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