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methyl 2-aminopyrazolo[1,5-a]pyridine-3-carboxylate hydrochloride
$325.00
CAS No.: 2706174-60-7
Catalog No.: 192907
Purity: 95%
MF: C9H10ClN3O2
MW: 227.651
Storage: 2-8 degree Celsius
SMILES: Cl.NC1=NN2C(C=CC=C2)=C1C(=O)OC
Catalog No.: 192907
Purity: 95%
MF: C9H10ClN3O2
MW: 227.651
Storage: 2-8 degree Celsius
SMILES: Cl.NC1=NN2C(C=CC=C2)=C1C(=O)OC
methyl 2-aminopyrazolo[1,5-a]pyridine-3-carboxylate hydrochloride; CAS No.: 2706174-60-7; methyl 2-aminopyrazolo[1,5-a]pyridine-3-carboxylate hydrochloride. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C9H10N4O {HCl and a molecular weight of 230.66 g/mol. It demonstrates a melting point in the range of 198-202 C and shows good solubility in water and common polar solvents like 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 protocols should be followed, including the use of protective gloves and eye wear, as methyl 2-aminopyrazolo[1,5-a]pyridine-3-carboxylate hydrochloride may cause skin and eye irritation. The amino group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, methyl 2-aminopyrazolo[1,5-a]pyridine-3-carboxylate hydrochloride serves as a key intermediate for synthesizing antidepressant agents, as documented in pharmaceutical research focusing on serotonergic compounds. Its amino substituent enables formation of bioactive amides through amidation reactions. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrazolopyridine ring system also facilitates coordination with metal ions, making it valuable for creating coordination polymers in materials science applications, as evidenced by structural chemistry publications.
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