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Spiroindoline

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Identification
Molecular formula
C11H16N2O2
CAS number
4765-16-8
IUPAC name
3-allyl-1,3-diazaspiro[4.6]undecane-2,4-dione
State
State

At room temperature, it is a solid.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
194.25g/mol
Molar mass
194.2470g/mol
Density
1.1320g/cm3
Appearence

The compound typically appears as a white crystalline solid. It may have a slight odor characteristic of amines or spiro compounds.

Comment on solubility

Solubility of 3-allyl-1,3-diazaspiro[4.6]undecane-2,4-dione

The solubility of 3-allyl-1,3-diazaspiro[4.6]undecane-2,4-dione can be influenced by several factors, including its molecular structure and the presence of functional groups. Here are some key points to consider:

  • Polarity: The presence of nitrogen atoms in the diazaspiro structure contributes to the molecule's polarity, which can enhance its solubility in polar solvents.
  • Saturation: The saturated spiro structure may hinder solubility in non-polar solvents due to steric hindrance.
  • Solvent Interactions: This compound may demonstrate varying solubility in different solvents, such as:
    • Water: Limited solubility is expected due to hydrophobic regions.
    • Alcohols: Increased solubility in ethanol or methanol can be observed due to hydrogen bonding.
    • Organic solvents: Soluble in solvents like dichloromethane or acetone, which can better accommodate its non-polar characteristics.

In summary, 3-allyl-1,3-diazaspiro[4.6]undecane-2,4-dione exhibits solubility that is dependent on the solvent properties, reflecting the compound's unique structural features. Understanding these interactions is crucial for applications in various chemical environments.

Interesting facts

Interesting Facts about 3-Allyl-1,3-Diazaspiro[4.6]undecane-2,4-dione

The compound 3-Allyl-1,3-diazaspiro[4.6]undecane-2,4-dione is a fascinating example of a spiro compound, displaying a unique and complex structure that emerges from the fusion of two rings. Here are some key points of interest:

  • Spiral Structure: The term "spiro" denotes that it contains a distinctive spirocyclic framework, combining two rings that share a single atom. This arrangement can impart specific steric and electronic properties, making such compounds interesting in drug design and materials science.
  • Divergence in Chemistry: Compounds with diaza substituents, such as this one, can exhibit divergent reactivity and serve as potential intermediates in various chemical reactions.
  • Biological Relevance: Various spiro compounds have been investigated for their biological activity. Due to the presence of the allyl group, there is potential for this compound to exhibit interesting pharmacological properties, warranting further studies.
  • Allied Studies: Research continues into synthetic methodologies for creating complex diazaspiro compounds, highlighting the challenges and excitement in organic synthesis. As scientists, we often quote the legendary chemist "In chemistry, the only constant is change."

With such a unique structural configuration along with its potential reactivity, 3-Allyl-1,3-diazaspiro[4.6]undecane-2,4-dione opens intriguing pathways for both academic research and industrial applications.

Synonyms
718-81-0
1,3-DIAZASPIRO(4.6)UNDECANE-2,4-DIONE, 3-ALLYL-
BRN 0790048
3'-Allylcycloheptanespiro-5'-hydantoin
DTXSID10222054