4-bromo-5-methylpyrazolo[1,5-a]pyridine

4-bromo-5-methylpyrazolo[1,5-a]pyridine

4,6-dichloropyrazolo[1,5-a]pyridine

4,6-dichloropyrazolo[1,5-a]pyridine

4-fluoropyrazolo[1,5-a]pyridine-3-carboxylic acid

$300.00
CAS No.: 1352625-33-2
Catalog No.: 192897
Purity: 95%
MF: C8H5FN2O2
MW: 180.138
Storage: 2-8 degree Celsius
SMILES: FC=1C=2N(C=CC1)N=CC2C(=O)O
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192897
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4-fluoropyrazolo[1,5-a]pyridine-3-carboxylic acid; CAS No.: 1352625-33-2; 4-fluoropyrazolo[1,5-a]pyridine-3-carboxylic acid. PROPERTIES: This compound appears as a white to off-white crystalline solid with molecular formula C8H5FN2O2 and a molecular weight of 186.14 g/mol. It exhibits a melting point in the range of 178-182 C and demonstrates moderate solubility in polar solvents such as water and methanol. The substance is hygroscopic and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at room temperature with protection from moisture and light. When handling, standard laboratory safety precautions should be observed, including the use of gloves and eye protection, as 4-fluoropyrazolo[1,5-a]pyridine-3-carboxylic acid may release irritating vapors upon heating. The carboxylic acid group requires careful handling in strongly basic environments. APPLICATIONS: In medicinal chemistry, 4-fluoropyrazolo[1,5-a]pyridine-3-carboxylic acid serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its fluorine substituent enables improved metabolic stability in biological systems. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in metal coordination chemistry for creating luminescent sensors, as reported in inorganic chemistry journals. The pyrazolopyridine ring system also facilitates formation of metal-organic frameworks (MOFs), making it valuable for gas storage applications in materials science, as evidenced by studies in crystallography publications.

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