3,9-Diazaspiro[5.5]undecan-2-one is a bicyclic compound characterized by its unique spiro structure, which consists of two fused rings sharing a single atom. This compound features two nitrogen atoms incorporated into its framework, contributing to its diaza designation. The presence of a carbonyl group (ketone) at the 2-position enhances its reactivity and potential for forming various derivatives. Typically, compounds like this exhibit interesting biological activities, making them of interest in medicinal chemistry and drug development. The spirocyclic nature often leads to unique conformational properties, influencing their interaction with biological targets. Additionally, the compound's solubility, stability, and reactivity can vary based on the functional groups present and the overall molecular structure. As with many nitrogen-containing heterocycles, it may participate in hydrogen bonding and other intermolecular interactions, which can affect its physical properties and potential applications. Overall, 3,9-diazaspiro[5.5]undecan-2-one represents a fascinating area of study within organic and medicinal chemistry.

3,9-diazaspiro[5.5]undecan-2-one

867006-20-0: 3,9-Diazaspiro[5.5]undecan-2-one is a bicyclic compound characterized by its unique spiro structure, which consists of two fused rings sharing a single atom. This compound features two nitrogen atoms incorporated into its framework, contributing to its diaza designation. The presence of a carbonyl group (ketone) at the 2-position enhances its reactivity and potential for forming various derivatives. Typically, compounds like this exhibit interesting biological activities, making them of interest in medicinal chemistry and drug development. The spirocyclic nature often leads to unique conformational properties, influencing their interaction with biological targets. Additionally, the compound's solubility, stability, and reactivity can vary based on the functional groups present and the overall molecular structure. As with many nitrogen-containing heterocycles, it may participate in hydrogen bonding and other intermolecular interactions, which can affect its physical properties and potential applications. Overall, 3,9-diazaspiro[5.5]undecan-2-one represents a fascinating area of study within organic and medicinal chemistry.

CAS 867006-20-0

3,9-diazaspiro[5.5]undecan-2-one

3,9-Diazaspiro[5.5]undecan-2-one

Ref: IN-DA008F94

3,9-Diazaspiro[5.5]undecan-2-one

Ref: 54-OR306347

3,9-DIAZASPIRO[5.5]UNDECAN-2-ONE

Ref: 10-F075876