Cas no 362661-88-9 (Pyrazolo[1,5-a]pyridine-6-methanol)

Pyrazolo[1,5-a]pyridine-6-methanol is a heterocyclic compound featuring a pyrazolo[1,5-a]pyridine core with a hydroxymethyl substituent at the 6-position. This structure serves as a versatile intermediate in pharmaceutical and agrochemical synthesis, offering opportunities for further functionalization due to its reactive alcohol group. Its fused bicyclic framework enhances molecular rigidity, which can be advantageous in the design of bioactive compounds with improved binding affinity and metabolic stability. The compound's well-defined synthetic route and high purity make it suitable for research applications in medicinal chemistry, particularly in the development of kinase inhibitors and other targeted therapeutics.
Pyrazolo[1,5-a]pyridine-6-methanol structure
362661-88-9 structure
Product Name:Pyrazolo[1,5-a]pyridine-6-methanol
CAS No:362661-88-9
MF:C8H8N2O
MW:148.16192150116
CID:4827050
PubChem ID:10931587
Update Time:2026-02-27

Pyrazolo[1,5-a]pyridine-6-methanol Chemical and Physical Properties

Names and Identifiers

    • pyrazolo[1,5-a]pyridin-6-ylmethanol
    • Pyrazolo[1,5-a]pyridine-6-methanol
    • SCHEMBL22715292
    • 362661-88-9
    • DB-144437
    • Inchi: 1S/C8H8N2O/c11-6-7-1-2-8-3-4-9-10(8)5-7/h1-5,11H,6H2
    • InChI Key: NJOUFCWSJNYISL-UHFFFAOYSA-N
    • SMILES: OCC1C=CC2=CC=NN2C=1

Computed Properties

  • Exact Mass: 148.063662883g/mol
  • Monoisotopic Mass: 148.063662883g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1
  • Complexity: 140
  • 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: 0.2
  • Topological Polar Surface Area: 37.5

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Additional information on Pyrazolo[1,5-a]pyridine-6-methanol

Pyrazolo[1,5-a]pyridine-6-methanol (CAS No. 362661-88-9): A Key Intermediate in Modern Pharmaceutical Research

The compound Pyrazolo[1,5-a]pyridine-6-methanol, identified by its unique Chemical Abstracts Service (CAS) number CAS No. 362661-88-9, represents a significant intermediate in the realm of pharmaceutical chemistry. This heterocyclic compound, featuring a fused pyrazole and pyridine core, has garnered considerable attention due to its versatile structural framework and potential applications in drug discovery and development.

Pyrazolo[1,5-a]pyridine derivatives are known for their broad spectrum of biological activities, making them valuable scaffolds for designing novel therapeutic agents. The methanol substituent at the 6-position of the pyrazolo[1,5-a]pyridine ring enhances the compound's reactivity and functionalization potential, allowing for further chemical modifications that can tailor its pharmacological properties.

In recent years, significant advancements have been made in leveraging this compound for the development of innovative drugs. Researchers have explored its utility in creating molecules with antimicrobial, anti-inflammatory, and anticancer properties. The structural flexibility of Pyrazolo[1,5-a]pyridine-6-methanol enables the synthesis of derivatives that can interact with various biological targets, thereby opening new avenues for therapeutic intervention.

One of the most compelling aspects of Pyrazolo[1,5-a]pyridine-6-methanol is its role in the synthesis of kinase inhibitors. Kinases are enzymes that play a crucial role in cell signaling pathways, and their dysregulation is often associated with various diseases, including cancer. By designing analogs of this compound that can selectively inhibit specific kinases, scientists aim to develop more effective and targeted therapies.

Recent studies have highlighted the potential of Pyrazolo[1,5-a]pyridine-6-methanol in developing treatments for neurological disorders. The compound's ability to cross the blood-brain barrier and interact with central nervous system receptors makes it an attractive candidate for drugs targeting conditions such as Alzheimer's disease and Parkinson's disease. Researchers are currently investigating its effects on neurotransmitter systems and its potential to modulate neuronal activity.

The methanol moiety in Pyrazolo[1,5-a]pyridine-6-methanol also plays a crucial role in its solubility and bioavailability. This feature is particularly important for pharmaceutical applications, as it ensures that the compound can be effectively delivered to target tissues in the body. Additionally, the methanol group provides a site for further functionalization, allowing chemists to modify the compound's properties to optimize its pharmacokinetic profile.

In conclusion, Pyrazolo[1,5-a]pyridine-6-methanol (CAS No. 362661-88-9) is a multifaceted compound with significant potential in pharmaceutical research. Its unique structural features and biological activities make it a valuable tool for developing novel therapeutic agents across various disease areas. As research continues to uncover new applications for this compound, it is likely to remain a cornerstone of drug discovery efforts in the coming years.

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