methyl 3-formyl-1-trityl-1H-pyrazole-4-carboxylate
$450.00
CAS No.: 960234-85-9
Catalog No.: 192884
Purity: 95%
MF: C25H20N2O3
MW: 396.446
Storage: 2-8 degree Celsius
SMILES: C(=O)C1=NN(C=C1C(=O)OC)C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
Catalog No.: 192884
Purity: 95%
MF: C25H20N2O3
MW: 396.446
Storage: 2-8 degree Celsius
SMILES: C(=O)C1=NN(C=C1C(=O)OC)C(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1
methyl 3-formyl-1-trityl-1H-pyrazole-4-carboxylate; CAS No.: 960234-85-9; methyl 3-formyl-1-trityl-1H-pyrazole-4-carboxylate. PROPERTIES: This compound presents as a pale yellow crystalline solid with molecular formula C24H20N2O3 and a molecular weight of 388.42 g/mol. It exhibits a melting point in the range of 132-136 C and demonstrates moderate solubility in common organic solvents like dichloromethane and tetrahydrofuran. 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 precautions should be observed, including the use of gloves and eye protection, as methyl 3-formyl-1-trityl-1H-pyrazole-4-carboxylate may release irritating vapors upon heating. The formyl group requires careful handling in strongly basic environments. APPLICATIONS: In medicinal chemistry, methyl 3-formyl-1-trityl-1H-pyrazole-4-carboxylate serves as a protected aldehyde intermediate for synthesizing anticancer agents, as documented in pharmaceutical research focusing on kinase inhibitors. Its trityl substituent enables controlled deprotection strategies in multi-step syntheses. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential 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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