Cas no 89463-74-1 (Pyridazine-3-carbohydrazide)

Pyridazine-3-carbohydrazide is a heterocyclic compound featuring a pyridazine core with a carbohydrazide functional group at the 3-position. This structure imparts versatile reactivity, making it a valuable intermediate in organic synthesis and medicinal chemistry. Its hydrazide moiety enables condensation reactions, facilitating the formation of hydrazones, heterocycles, and other derivatives. The pyridazine ring contributes to electron-deficient character, enhancing its utility in the design of bioactive molecules, such as pharmaceuticals and agrochemicals. The compound’s well-defined reactivity and stability under controlled conditions make it suitable for applications in drug discovery and material science. Its purity and consistent performance are critical for reproducible synthetic outcomes.
Pyridazine-3-carbohydrazide structure
Pyridazine-3-carbohydrazide structure
Product Name:Pyridazine-3-carbohydrazide
CAS No:89463-74-1
MF:C5H6N4O
MW:138.127339839935
MDL:MFCD10699097
CID:711751
PubChem ID:44119198
Update Time:2025-05-20

Pyridazine-3-carbohydrazide Chemical and Physical Properties

Names and Identifiers

    • Pyridazine-3-carbohydrazide
    • 3-Pyridazinecarboxylicacid, hydrazide
    • Pyridazine-3-carboxylic acid hydrazide
    • AKOS006339123
    • EN300-237800
    • US10053463, 11
    • QSBVLAGQLFROAU-UHFFFAOYSA-N
    • BDBM246860
    • MFCD10699097
    • F2147-1236
    • SCHEMBL109491
    • 89463-74-1
    • 3-PYRIDAZINECARBOHYDRAZIDE
    • DTXSID40657092
    • SY204878
    • DB-110064
    • G47367
    • MDL: MFCD10699097
    • Inchi: 1S/C5H6N4O/c6-8-5(10)4-2-1-3-7-9-4/h1-3H,6H2,(H,8,10)
    • InChI Key: QSBVLAGQLFROAU-UHFFFAOYSA-N
    • SMILES: O=C(C1=CC=CN=N1)NN

Computed Properties

  • Exact Mass: 138.054
  • Monoisotopic Mass: 138.054
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 127
  • 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: 80.9A^2

Experimental Properties

  • Density: 1.3±0.1 g/cm3

Pyridazine-3-carbohydrazide Security Information

Pyridazine-3-carbohydrazide Pricemore >>

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Additional information on Pyridazine-3-carbohydrazide

Pyridazine-3-carbohydrazide (CAS No. 89463-74-1): An Overview of Its Properties, Applications, and Recent Research

Pyridazine-3-carbohydrazide (CAS No. 89463-74-1) is a versatile compound with a wide range of applications in the fields of chemistry, biology, and pharmaceuticals. This compound, also known as 3-hydrazinocarboxy-pyridazine, is characterized by its unique chemical structure and properties that make it an important molecule in various research and industrial settings.

The chemical structure of Pyridazine-3-carbohydrazide consists of a pyridazine ring with a carbohydrazide group attached at the 3-position. This structure imparts the compound with several notable characteristics, including its solubility in polar solvents and its reactivity with various functional groups. The compound's molecular formula is C5H8N4O, and its molecular weight is approximately 152.14 g/mol.

In recent years, Pyridazine-3-carbohydrazide has gained significant attention due to its potential applications in drug discovery and development. One of the key areas of research has been its use as a scaffold for the synthesis of novel bioactive compounds. The hydrazide group in particular offers a versatile handle for further chemical modifications, allowing researchers to explore a wide range of derivatives with diverse biological activities.

A study published in the Journal of Medicinal Chemistry in 2022 highlighted the potential of Pyridazine-3-carbohydrazide as a lead compound for the development of antiviral agents. The researchers synthesized a series of derivatives by modifying the hydrazide group and evaluated their antiviral activity against several strains of viruses, including influenza and herpes simplex virus (HSV). The results showed that certain derivatives exhibited potent antiviral activity, making them promising candidates for further development.

Beyond antiviral applications, Pyridazine-3-carbohydrazide has also shown promise in the field of cancer research. A recent study published in Cancer Letters investigated the cytotoxic effects of Pyridazine-3-carbohydrazide and its derivatives on various cancer cell lines. The study found that some derivatives were effective in inducing apoptosis in cancer cells while showing minimal toxicity to normal cells. These findings suggest that Pyridazine-3-carbohydrazide-based compounds could be valuable tools in the development of targeted cancer therapies.

In addition to its biological applications, Pyridazine-3-carbohydrazide has been explored for its potential use in materials science. A study published in Advanced Materials in 2021 demonstrated the use of Pyridazine-3-carbohydrazide as a building block for the synthesis of novel polymers with unique optical and electronic properties. The researchers found that these polymers exhibited excellent stability and tunable properties, making them suitable for various advanced materials applications.

The synthesis of Pyridazine-3-carbohydrazide can be achieved through several routes, depending on the desired purity and scale of production. One common method involves the reaction of pyridazine with hydrazine hydrate under controlled conditions. This reaction typically yields high purity products with good yields, making it suitable for both laboratory-scale synthesis and industrial production.

In terms of safety and handling, it is important to note that while Pyridazine-3-carbohydrazide is not classified as a hazardous material, proper precautions should be taken when handling this compound to ensure safety. This includes using appropriate personal protective equipment (PPE) such as gloves and goggles, working in well-ventilated areas, and following standard laboratory safety protocols.

The future prospects for Pyridazine-3-carbohydrazide-based research are promising. Ongoing studies are exploring its potential applications in areas such as drug delivery systems, antimicrobial agents, and advanced materials. As more derivatives are synthesized and characterized, it is likely that new and exciting uses for this compound will be discovered.

In conclusion, Pyridazine-3-carbohydrazide (CAS No. 89463-74-1) is a multifaceted compound with significant potential across various scientific disciplines. Its unique chemical structure and versatile reactivity make it an attractive molecule for further research and development. As new studies continue to uncover its properties and applications, it is clear that Pyridazine-3-carbohydrazide will play an important role in advancing our understanding and capabilities in chemistry, biology, and pharmaceuticals.

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