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7-benzyl-4,7-diazaspiro[2.5]octane-5,8-dione
$300.00
CAS No.: 1222106-43-5
Catalog No.: WLZ1197
Purity: 95%
MF: C13H14N2O2
MW: 230.267
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1CC(NC2(CC2)C1=O)=O
Catalog No.: WLZ1197
Purity: 95%
MF: C13H14N2O2
MW: 230.267
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1CC(NC2(CC2)C1=O)=O
CAS NO.: 1222106-43-5; 7-benzyl-4,7-diazaspiro[2.5]octane-5,8-dione. PROPERTIES: This spirocyclic diamide features a benzyl group attached to a nitrogen atom in a 4,7-diazaspiro[2.5]octane framework with two amide functionalities, creating a molecule with potential pharmacological relevance. The 7-benzyl-4,7-diazaspiro[2.5]octane-5,8-dione 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 rigid spirocycle that imparts specific three-dimensional geometry, which may facilitate receptor interactions. 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 accidental spillage, clean the area with a damp cloth and dispose of materials according to local regulations. APPLICATIONS: The 7-benzyl-4,7-diazaspiro[2.5]octane-5,8-dione serves as a lead compound in medicinal chemistry research targeting central nervous system disorders. Its spirocyclic structure and benzyl substitution make it suitable for developing small molecule inhibitors of specific protein-protein interactions. In pharmaceutical development, this compound functions as a starting material for synthesizing benzyl-substituted spiropiperidines with potential antipsychotic and anxiolytic activities. 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 neuropsychiatric conditions.
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