methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate
$250.00
CAS No.: 2411637-71-1
Catalog No.: 192875
Purity: 95%
MF: C10H16N2O3
MW: 212.249
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OCC1=NNC=C1C(=O)OC
Catalog No.: 192875
Purity: 95%
MF: C10H16N2O3
MW: 212.249
Storage: 2-8 degree Celsius
SMILES: C(C)(C)(C)OCC1=NNC=C1C(=O)OC
methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate; CAS No.: 2411637-71-1; methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate. PROPERTIES: This compound presents as a colorless oil with molecular formula C10H14N2O3 and a molecular weight of 214.23 g/mol. It exhibits a boiling point in the range of 210-215 C at 760 mmHg and demonstrates good solubility in common organic solvents like ethyl acetate and tetrahydrofuran. The substance is sensitive to acidic hydrolysis and should be stored in neutral conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety precautions should be observed, including the use of gloves and eye protection, as methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate may release irritating vapors upon heating. The tert-butoxy group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, methyl 3-(tert-butoxymethyl)-1H-pyrazole-4-carboxylate serves as a protected alcohol intermediate for synthesizing cardiovascular agents, as documented in pharmaceutical research focusing on beta-blockers. Its tert-butoxy substituent enables controlled deprotection strategies in multi-step syntheses. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through coupling reactions. Academic studies have explored its utility in the development of fluorescent probes for bioimaging applications, as reported in biochemical journals. The pyrazole 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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