CAS 117782-76-0
:Pyrazolo[1,5-a]pyridin-3-ylmethanol
Description:
Pyrazolo[1,5-a]pyridin-3-ylmethanol is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both pyrazole and pyridine moieties. This compound features a hydroxymethyl group (-CH2OH) attached to the pyridine ring, contributing to its potential reactivity and solubility in various solvents. It is typically a white to off-white solid, and its molecular structure allows for various interactions, making it of interest in medicinal chemistry and drug development. The presence of the hydroxymethyl group can influence its biological activity, potentially enhancing its ability to interact with biological targets. Pyrazolo[1,5-a]pyridin-3-ylmethanol may exhibit properties such as moderate to high polarity, which can affect its pharmacokinetics and bioavailability. Additionally, the compound may participate in hydrogen bonding due to the hydroxyl group, further influencing its chemical behavior and interactions. Overall, this compound is significant in research contexts, particularly in the exploration of new therapeutic agents.
Formula:C8H8N2O
InChI:InChI=1/C8H8N2O/c11-6-7-5-9-10-4-2-1-3-8(7)10/h1-5,11H,6H2
SMILES:c1ccn2c(c1)c(cn2)CO
Synonyms:- Pyrazolo[1,5-a]pyridine-3-methanol
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Found 4 products.
Pyrazolo[1,5-a]pyridine-3-methanol
CAS:Formula:C8H8N2OPurity:97%Color and Shape:SolidMolecular weight:148.1619Pyrazolo[1,5-a]pyridin-3-ylmethanol
CAS:<p>Pyrazolo[1,5-a]pyridin-3-ylmethanol</p>Purity:97%Molecular weight:148.16g/mol(H-Pyrazolo[1,5-a]pyridin-3-yl)methanol
CAS:<p>Pyrazolopyridazine is a compound that has antiparasitic and antibiotic properties. It is used as an antiparasitic drug in the treatment of roundworm, hookworm, whipworm, and tapeworm infections. Pyrazolopyridazine is also used to treat bacterial infections such as tuberculosis. This drug has been shown to be effective against both Gram-positive and Gram-negative bacteria. Pyrazolopyridazine also exhibits antiviral properties against HIV-1 (human immunodeficiency virus) replication in human lymphocytes in vitro. The synthetic pathway of pyrazolopyridazine involves the condensation of 2-aminoacetophenone with 3-chloro-5-(2,4,6-trichlorophenyl)-pyridine followed by reaction with ammonia to give 3-amino-N-(2,4,6-trichlorophenyl)pyrazole.<br>Pyrazolopyr</p>Formula:C8H8N2OPurity:Min. 95%Molecular weight:148.16 g/mol




