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Nitrendipine

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Identification
Molecular formula
C15H20N2
CAS number
21898-19-1
IUPAC name
4-(diethylamino)-2-(1-naphthyl)butanenitrile
State
State

This compound is typically a solid at room temperature.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
496.20
Boiling point (Kelvin)
769.35
General information
Molecular weight
220.33g/mol
Molar mass
360.4750g/mol
Density
1.1205g/cm3
Appearence

Nitrendipine typically appears as a yellow crystalline solid.

Comment on solubility

Solubility of 4-(diethylamino)-2-(1-naphthyl)butanenitrile

The solubility of 4-(diethylamino)-2-(1-naphthyl)butanenitrile can be influenced by various factors, including its chemical structure and the solvent used. This compound, characterized by its large non-polar naphthyl group and polar diethylamino group, exhibits intriguing solubility properties:

  • Polar Solvents: It tends to have improved solubility in polar solvents such as water and alcohols due to the presence of the diethylamino functional group.
  • Non-Polar Solvents: Conversely, it is likely to be soluble in non-polar solvents owing to its hydrophobic naphthyl group, which favors interactions with similar non-polar molecules.
  • Temperature Influence: As with many organic compounds, solubility may increase with temperature, allowing for the dissolution of greater quantities of the substance in a given solvent.

In summary, understanding the solubility of this compound is crucial for applications in synthesis and formulation, as it enables scientists to optimize conditions for reaction and product isolation. Experimentation will be key in determining the exact solubility, as empirical data often provides the best insight into how a compound behaves in different environments.

Interesting facts

Interesting Facts about 4-(Diethylamino)-2-(1-naphthyl)butanenitrile

4-(Diethylamino)-2-(1-naphthyl)butanenitrile, often referred to in the scientific community for its unique structure and properties, is a fascinating compound with several intriguing aspects:

  • Biological Activity: This compound has been studied for its potential biological activities, including applications in pharmacology and medicinal chemistry. It shows promise as a selective ligand, which may open avenues for research in drug development.
  • Structural Diversity: The presence of the diethylamino and naphthyl groups creates a structurally diverse molecule that can interact in unique ways with biological targets, making it a subject of interest in the realm of molecular design.
  • Pharmacophore: Due to its functional groups, the compound may act as a pharmacophore, an essential feature for developing new therapeutic agents that target specific receptors or enzymes.
  • Synthetic Techniques: The synthesis of this compound often involves advanced organic chemistry techniques, including nucleophilic substitution and cyclization reactions. Mastery of these synthetic methodologies is crucial for chemists aiming to create similar or complex compounds.
  • Research Potential: There is ongoing research into the properties and potential applications of this compound in various fields, including materials science and chemical biology, which may lead to innovative uses in technology and medicine.

This compound exemplifies the rich interplay between chemistry, biology, and materials science, paving the way for future discoveries and advancements. As research continues, it will be exciting to see how compounds like 4-(diethylamino)-2-(1-naphthyl)butanenitrile can contribute to our understanding of chemical interactions and drug design.

Synonyms
2572-73-8
BRN 2128838
alpha-(2-(Diethylamino)ethyl)-1-naphthaleneacetonitrile
1-NAPHTHALENEACETONITRILE, alpha-(2-(DIETHYLAMINO)ETHYL)-
SCHEMBL10566588
DTXSID70948602
OTKDXFJFXVASII-UHFFFAOYSA-N
4-(N,N-diethylamino)-2-(1-naphthyl)butyronitrile
4-(DIETHYLAMINO)-2-(NAPHTHALEN-1-YL)BUTANENITRILE