Cas no 1073488-86-4 (6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester)

6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester structure
1073488-86-4 structure
Product Name:6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester
CAS No:1073488-86-4
MF:C7H9ClN4O2
MW:216.62495970726
MDL:MFCD29072106
CID:1098106
PubChem ID:59363340
Update Time:2025-11-02

6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester Chemical and Physical Properties

Names and Identifiers

    • 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester
    • ethyl 6-chloro-3-hydrazinylpyridazine-4-carboxylate
    • MFCD29072106
    • 6-Chloro-3-hydrazino-pyridazine-4-carboxylic acid ethyl ester
    • 1073488-86-4
    • 6-Chloro-3-hydrazinopyridazine-4-carboxylic acid ethyl ester
    • SCHEMBL137020
    • Ethyl6-chloro-3-hydrazinylpyridazine-4-carboxylate
    • QDRNORRKAVFHOB-UHFFFAOYSA-N
    • MDL: MFCD29072106
    • Inchi: 1S/C7H9ClN4O2/c1-2-14-7(13)4-3-5(8)11-12-6(4)10-9/h3H,2,9H2,1H3,(H,10,12)
    • InChI Key: QDRNORRKAVFHOB-UHFFFAOYSA-N
    • SMILES: ClC1=CC(C(=O)OCC)=C(N=N1)NN

Computed Properties

  • Exact Mass: 216.0414032g/mol
  • Monoisotopic Mass: 216.0414032g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 4
  • Complexity: 204
  • 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: 1.1
  • Topological Polar Surface Area: 90.1?2

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Additional information on 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester

Comprehensive Overview of 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester (CAS No. 1073488-86-4)

6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester (CAS No. 1073488-86-4) is a specialized organic compound that has garnered significant attention in pharmaceutical and agrochemical research. This compound, characterized by its pyridazine core, is a versatile intermediate in the synthesis of bioactive molecules. Researchers are increasingly exploring its potential due to its unique hydrazinyl and ester functional groups, which enable diverse chemical modifications. The 6-chloro substitution further enhances its reactivity, making it a valuable building block for drug discovery and material science applications.

In recent years, the demand for pyridazine derivatives has surged, driven by their role in developing novel therapeutics. For instance, 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester is being investigated for its potential in designing kinase inhibitors, a hot topic in oncology research. Kinase inhibitors are pivotal in targeted cancer therapies, and the structural flexibility of this compound allows for the creation of tailored molecules. Additionally, its ethyl ester group improves solubility, a critical factor in drug formulation, addressing a common challenge in pharmaceutical development.

The compound’s CAS No. 1073488-86-4 is frequently searched in academic and industrial databases, reflecting its growing relevance. Users often inquire about its synthetic routes, physicochemical properties, and applications in medicinal chemistry. For example, questions like "How to synthesize 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester?" or "What are the uses of pyridazine-based compounds in drug design?" highlight the compound’s interdisciplinary appeal. These queries align with broader trends in green chemistry and sustainable synthesis, as researchers seek eco-friendly methods to produce such intermediates.

Another area of interest is the compound’s role in agrochemical innovation. With the global push for sustainable agriculture, 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester is being studied for its potential as a precursor to herbicides and pesticides. Its chloro and hydrazinyl moieties offer sites for structural optimization, enabling the development of safer and more efficient agrochemicals. This aligns with the increasing demand for low-toxicity and high-efficacy crop protection solutions.

From a technical perspective, the compound’s molecular weight, melting point, and spectral data (e.g., NMR, IR) are critical for quality control and regulatory compliance. Laboratories often prioritize these parameters to ensure reproducibility in synthetic processes. Moreover, the rise of computational chemistry tools has facilitated virtual screening of pyridazine derivatives, accelerating the identification of promising candidates for further experimentation.

In conclusion, 6-chloro-3-hydrazinyl-4-Pyridazinecarboxylic acid ethyl ester (CAS No. 1073488-86-4) represents a multifaceted compound with broad applications in pharmaceuticals, agrochemicals, and material science. Its structural features and adaptability make it a focal point for researchers addressing contemporary challenges in drug development and sustainable chemistry. As the scientific community continues to explore its potential, this compound is poised to play a pivotal role in advancing innovation across multiple industries.

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