3-bromo-1H-pyrazolo[3,4-c]pyridin-7(6H)-one

3-bromo-1H-pyrazolo[3,4-c]pyridin-7(6H)-one

methyl 4,6-dichloropyrazolo[1,5-a]pyridine-3-carboxylate

methyl 4,6-dichloropyrazolo[1,5-a]pyridine-3-carboxylate

3-bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine

$325.00
CAS No.: 957760-22-4
Catalog No.: 192912
Purity: 95%
MF: C6H3BrClN3
MW: 232.468
Storage: 2-8 degree Celsius
SMILES: BrC1=NNC2=C(N=CC=C21)Cl
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3-bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine; CAS No.: 957760-22-4; 3-bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine. PROPERTIES: This compound presents as a white to off-white crystalline solid with molecular formula C7H4BrClN3 and a molecular weight of 229.52 g/mol. It exhibits a melting point in the range of 178-182 C and demonstrates moderate solubility in common organic solvents like dichloromethane and acetone. The substance is sensitive to photodegradation and should be stored in amber containers. Recommended storage involves maintaining in tightly sealed containers at temperatures below 20 C, protected from light and moisture. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as 3-bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine may release toxic fumes upon heating. The bromo and chloro groups require careful handling in strongly basic environments. APPLICATIONS: In the pharmaceutical industry, 3-bromo-7-chloro-1H-pyrazolo[3,4-c]pyridine serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on pyrazole derivatives. Its bromo and chloro substituents enable participation in cross-coupling reactions for constructing biaryl systems. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through nucleophilic aromatic substitution reactions. Academic research has explored its potential in the development of fluorescent probes for bioimaging applications, as reported in biochemical journals. The pyrazolopyridine ring system also facilitates coordination with metal ions, making it valuable for creating luminescent materials in materials science applications, as evidenced by inorganic chemistry publications.

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