Cas no 5423-20-1 (1H-Imidazole-4,5-dicarbohydrazide)

1H-Imidazole-4,5-dicarbohydrazide is a heterocyclic compound featuring an imidazole core functionalized with two carbohydrazide groups at the 4 and 5 positions. This structure imparts versatility in coordination chemistry and organic synthesis, making it a valuable intermediate for the development of chelating agents, pharmaceuticals, and polymeric materials. Its dual carbohydrazide moieties enhance metal-binding affinity, suitable for applications in catalysis or sensor design. The compound’s rigid imidazole backbone contributes to thermal and chemical stability, while its reactive hydrazide groups enable further derivatization. It is particularly useful in constructing heterocyclic frameworks or as a precursor for bioactive molecules, offering synthetic flexibility in research and industrial contexts.
1H-Imidazole-4,5-dicarbohydrazide structure
5423-20-1 structure
Product Name:1H-Imidazole-4,5-dicarbohydrazide
CAS No:5423-20-1
MF:C5H8N6O2
MW:184.156019210815
MDL:MFCD00723482
CID:376536
PubChem ID:72687
Update Time:2025-08-05

1H-Imidazole-4,5-dicarbohydrazide Chemical and Physical Properties

Names and Identifiers

    • 1H-Imidazole-4,5-dicarboxylicacid, dihydrazide (9CI)
    • 1H-Imidazole-4,5-dicarbohydrazide
    • 1H-Imidazole-4,5-di(carbohydrazide)
    • NSC 10005
    • NS00033007
    • NCIOpen2_000300
    • SR-01000596903
    • 5423-20-1
    • CS-0327030
    • AKOS000567247
    • DTXSID50202577
    • LS-09104
    • UW0S5PMS3T
    • IMIDAZOLE-4,5-DICARBOXYLIC ACID, DIHYDRAZIDE
    • SR-01000596903-1
    • NSC-64855
    • 1H-Imidazole-4,5-dicarboxylic acid, dihydrazide
    • EINECS 226-550-3
    • MFCD00723482
    • NSC64855
    • NSC10005
    • NSC-10005
    • UNII-UW0S5PMS3T
    • Oprea1_283753
    • MDL: MFCD00723482
    • Inchi: 1S/C5H8N6O2/c6-10-4(12)2-3(5(13)11-7)9-1-8-2/h1H,6-7H2,(H,8,9)(H,10,12)(H,11,13)
    • InChI Key: MBKVDEBREBZMCM-UHFFFAOYSA-N
    • SMILES: O=C(C1=C(C(NN)=O)N=CN1)NN

Computed Properties

  • Exact Mass: 184.071
  • Monoisotopic Mass: 184.071
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 5
  • Hydrogen Bond Acceptor Count: 8
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 219
  • 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: 139A^2
  • XLogP3: -2.2

Experimental Properties

  • Density: 1.587
  • Boiling Point: °Cat760mmHg
  • Flash Point: °C
  • Refractive Index: 1.679

1H-Imidazole-4,5-dicarbohydrazide Pricemore >>

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abcr
AB416053-500 mg
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Additional information on 1H-Imidazole-4,5-dicarbohydrazide

Comprehensive Overview of 1H-Imidazole-4,5-dicarbohydrazide (CAS No. 5423-20-1): Properties, Applications, and Innovations

1H-Imidazole-4,5-dicarbohydrazide (CAS No. 5423-20-1) is a specialized heterocyclic compound that has garnered significant attention in pharmaceutical and materials science research. This imidazole derivative features a unique molecular structure with two carbohydrazide functional groups, making it a versatile intermediate for synthesizing high-value compounds. Its chemical stability and reactivity have positioned it as a key player in drug discovery, polymer chemistry, and agrochemical development.

Recent trends in green chemistry and sustainable synthesis have amplified interest in 1H-Imidazole-4,5-dicarbohydrazide. Researchers are exploring its potential as a biocompatible linker for drug-delivery systems, particularly in cancer therapeutics and antimicrobial agents. The compound's ability to form stable coordination complexes with metal ions also makes it valuable for designing functional materials, such as MOFs (Metal-Organic Frameworks) and corrosion inhibitors.

From an industrial perspective, 1H-Imidazole-4,5-dicarbohydrazide is increasingly used in the production of high-performance polymers. Its dual hydrazide groups enable cross-linking reactions that enhance thermal stability and mechanical strength in polyimide resins—a critical requirement for aerospace and electronics applications. Innovations in 3D printing materials and flexible electronics further underscore its relevance in cutting-edge technologies.

The compound's pharmacological potential is another hot topic. Computational studies suggest that 1H-Imidazole-4,5-dicarbohydrazide derivatives may exhibit enzyme inhibitory activity, particularly against targets like tyrosine kinases and PARP enzymes. These findings align with the growing demand for precision medicine and targeted therapies. Additionally, its role in chemo-sensors for detecting heavy metals resonates with environmental monitoring needs.

Quality control and analytical methods for CAS No. 5423-20-1 are frequently discussed in scientific literature. Techniques like HPLC, NMR spectroscopy, and mass spectrometry are essential for verifying purity, given its applications in sensitive domains. Regulatory compliance, especially for GMP-grade synthesis, remains a priority for manufacturers.

In summary, 1H-Imidazole-4,5-dicarbohydrazide exemplifies the convergence of multidisciplinary research. Its adaptability across drug development, advanced materials, and environmental science ensures its continued relevance. As industries prioritize sustainability and innovation, this compound is poised to play a pivotal role in shaping future technologies.

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