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3-bromo-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazine
$300.00
CAS No.: 1393558-10-5
Catalog No.: WLZ1229
Purity: 95%
MF: C6H7BrN2O
MW: 203.039
Storage: 2-8 degree Celsius
SMILES: BrC=1C=NN2C1COCC2
Catalog No.: WLZ1229
Purity: 95%
MF: C6H7BrN2O
MW: 203.039
Storage: 2-8 degree Celsius
SMILES: BrC=1C=NN2C1COCC2
CAS NO.: 1393558-10-5; 3-bromo-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazine. PROPERTIES: This brominated heterocycle combines a bromine substituent with a partially hydrogenated pyrazolo[5,1-c][1,4]oxazine framework, creating a molecule with potential pharmacological relevance. The 3-bromo-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazine typically appears as a white to off-white crystalline solid with limited aqueous solubility but good solubility in polar aprotic solvents. Its molecular architecture includes a bromine atom that renders the molecule reactive toward nucleophilic substitution reactions. For optimal stability and to preserve its structural integrity, this compound should be stored at 2-8 degree Celsius in a desiccator under anhydrous conditions. When handling, researchers should employ standard laboratory safety practices including nitrile gloves and a lab coat. This compound is hygroscopic and may degrade upon exposure to moisture. In case of skin contact, wash thoroughly with soap and water; if eye contact occurs, rinse immediately and seek medical advice. APPLICATIONS: The 3-bromo-6,7-dihydro-4H-pyrazolo[5,1-c][1,4]oxazine serves as a lead compound in medicinal chemistry research targeting enzyme inhibitors and receptor modulators. The bromine substituent provides a bioisosteric replacement that can enhance target binding affinity and selectivity. In pharmaceutical development, this compound functions as a starting material for synthesizing antimicrobial and anticancer agents where the fused heterocycle contributes to target engagement. Additionally, the molecule finds utility in chemical biology studies where its unique scaffold can be used to probe enzyme inhibition mechanisms and cellular signaling pathways. Researchers utilizing this compound benefit from its defined stereochemistry and functional group arrangement, advancing investigations into novel therapeutic approaches for various disease conditions.
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