4-hydroxy-5,5,6-trimethyl-4,5-dihydropyridazin-3(2H)-one
$375.00
CAS No.: 1161737-36-5
Catalog No.: 192914
Purity: 95%
MF: C7H12N2O2
MW: 156.185
Storage: 2-8 degree Celsius
SMILES: OC1C(NN=C(C1(C)C)C)=O
Catalog No.: 192914
Purity: 95%
MF: C7H12N2O2
MW: 156.185
Storage: 2-8 degree Celsius
SMILES: OC1C(NN=C(C1(C)C)C)=O
4-hydroxy-5,5,6-trimethyl-4,5-dihydropyridazin-3(2H)-one; CAS No.: 1161737-36-5; 4-hydroxy-5,5,6-trimethyl-4,5-dihydropyridazin-3(2H)-one. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C6H9N2O2 and a molecular weight of 143.15 g/mol. It demonstrates a melting point in the range of 168-172 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to oxidation and should be stored under inert atmosphere. 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 4-hydroxy-5,5,6-trimethyl-4,5-dihydropyridazin-3(2H)-one may cause skin irritation. The hydroxyl group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, 4-hydroxy-5,5,6-trimethyl-4,5-dihydropyridazin-3(2H)-one serves as an intermediate for synthesizing cardiovascular agents, as described in medicinal chemistry literature focusing on beta-blockers. Its hydroxyl substituent enables formation of bioactive esters through esterification reactions. Additionally, this compound functions as a building block for preparing agrochemicals with insecticidal activities through formation of urea derivatives. Academic research has explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyridazinone 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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