Cas no 1360968-74-6 (5-methyl-1h-indazol-4-ol)

5-Methyl-1H-indazol-4-ol is a heterocyclic aromatic compound characterized by an indazole ring system fused with an imidazole structure. The specific substitution pattern includes a hydroxyl group at position 4 and a methyl substituent at position 5. This combination offers several notable features: the aromatic indazole core provides inherent stability, while the indazole-4-ol moiety possesses potential hydrogen bonding capabilities due to the hydroxyl group. The methyl substituent at C5 may influence pharmacokinetic properties or alter binding affinities in biological contexts compared to unsubstituted analogues. Its defined structure makes it a valuable synthetic intermediate or candidate molecule for research in medicinal chemistry, agrochemistry, or materials science due to its potential biological activity profile stemming from the indazole scaffold.
5-methyl-1h-indazol-4-ol structure
5-methyl-1h-indazol-4-ol structure
Product Name:5-methyl-1h-indazol-4-ol
CAS No:1360968-74-6
MF:C8H8N2O
MW:148.16192150116
MDL:MFCD22689684
CID:1244737
PubChem ID:135742473
Update Time:2025-06-16

5-methyl-1h-indazol-4-ol Chemical and Physical Properties

Names and Identifiers

    • 5-methyl-1h-indazol-4-ol
    • CS-0050443
    • 1360968-74-6
    • P17648
    • AKOS027424967
    • AS-54225
    • SB16390
    • 5-methyl-1,2-dihydroindazol-4-one
    • MFCD22689684
    • MDL: MFCD22689684
    • Inchi: 1S/C8H8N2O/c1-5-2-3-7-6(8(5)11)4-9-10-7/h2-4,11H,1H3,(H,9,10)
    • InChI Key: AYQJQJPZYLGUPN-UHFFFAOYSA-N
    • SMILES: OC1=C(C)C=CC2=C1C=NN2

Computed Properties

  • Exact Mass: 148.063662883g/mol
  • Monoisotopic Mass: 148.063662883g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 0
  • Complexity: 151
  • 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: 1.6
  • Topological Polar Surface Area: 48.9?2

5-methyl-1h-indazol-4-ol Pricemore >>

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Additional information on 5-methyl-1h-indazol-4-ol

Recent Advances in the Study of 5-methyl-1h-indazol-4-ol (CAS: 1360968-74-6) and Its Applications in Chemical Biology and Medicine

5-methyl-1h-indazol-4-ol (CAS: 1360968-74-6) has emerged as a compound of significant interest in the field of chemical biology and medicinal chemistry. Recent studies have highlighted its potential as a versatile scaffold for the development of novel therapeutic agents, particularly in the areas of oncology and inflammation. This research briefing provides an overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and potential applications.

A recent study published in the Journal of Medicinal Chemistry explored the synthesis and optimization of 5-methyl-1h-indazol-4-ol derivatives for enhanced pharmacokinetic properties. The researchers employed a multi-step synthetic route, starting from commercially available precursors, to achieve high yields and purity of the target compound. The study also investigated the compound's stability under various physiological conditions, providing valuable insights for future formulation development.

In the context of biological activity, 5-methyl-1h-indazol-4-ol has shown promising results as an inhibitor of key signaling pathways involved in cancer progression. A 2023 study in Cancer Research demonstrated that this compound effectively targets the PI3K/AKT/mTOR pathway, leading to significant inhibition of tumor growth in preclinical models. The researchers noted that the compound's unique structural features contribute to its selectivity and potency, making it a promising candidate for further development.

Another area of active research involves the application of 5-methyl-1h-indazol-4-ol in inflammatory diseases. A recent publication in Nature Communications reported that derivatives of this compound exhibit potent anti-inflammatory effects by modulating NF-κB signaling. The study utilized both in vitro and in vivo models to validate the compound's efficacy, with results suggesting potential applications in conditions such as rheumatoid arthritis and inflammatory bowel disease.

From a drug development perspective, the physicochemical properties of 5-methyl-1h-indazol-4-ol have been extensively characterized. Computational modeling studies have predicted favorable drug-like properties, including good solubility and membrane permeability. These findings, combined with the compound's demonstrated biological activity, position it as a strong candidate for lead optimization programs in pharmaceutical research.

Looking ahead, several research groups are exploring the potential of 5-methyl-1h-indazol-4-ol as a building block for more complex drug molecules. Its structural flexibility allows for diverse modifications, enabling the creation of libraries of derivatives with tailored biological activities. This approach aligns with current trends in medicinal chemistry that emphasize the importance of scaffold diversity in drug discovery.

In conclusion, the growing body of research on 5-methyl-1h-indazol-4-ol (CAS: 1360968-74-6) underscores its significance in contemporary chemical biology and medicinal chemistry. The compound's unique properties and demonstrated biological activities make it a valuable subject for ongoing research, with potential applications spanning multiple therapeutic areas. Future studies will likely focus on further optimizing its pharmacological profile and exploring its mechanisms of action in greater detail.

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