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4-(Dimethylamino)-2-(1-naphthyl)butanenitrile

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Identification
Molecular formula
C16H18N2
CAS number
54866-89-0
IUPAC name
4-(dimethylamino)-2-(1-naphthyl)butanenitrile
State
State

At room temperature, 4-(Dimethylamino)-2-(1-naphthyl)butanenitrile exists as a solid, characterized by its crystalline form and pale yellow appearance.

Melting point (Celsius)
48.50
Melting point (Kelvin)
321.65
Boiling point (Celsius)
321.00
Boiling point (Kelvin)
594.15
General information
Molecular weight
238.33g/mol
Molar mass
238.3280g/mol
Density
1.0590g/cm3
Appearence

4-(Dimethylamino)-2-(1-naphthyl)butanenitrile appears as a crystalline solid with a pale yellow color. It is known for its distinctive aromatic odor, attributed to the naphthyl group present in the structure.

Comment on solubility

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

The solubility of 4-(dimethylamino)-2-(1-naphthyl)butanenitrile can be influenced by numerous factors, including its molecular structure and the presence of functional groups. Here are some key points regarding its solubility:

  • Polarity: Given the presence of the dimethylamino group, the compound exhibits some polar characteristics, which can enhance its solubility in polar solvents like water to a limited extent.
  • Non-polar Influence: The naphthyl moiety contributes to non-polar characteristics, likely increasing solubility in non-polar organic solvents such as chloroform or ethyl acetate.
  • Organic Solvents: This compound is expected to dissolve well in solvents such as ethanol, acetone, and other organic solvents due to its overall hydrophobic properties.

In summary, while 4-(dimethylamino)-2-(1-naphthyl)butanenitrile may show moderate solubility in water, its solubility is significantly enhanced in non-polar and various organic solvents. This dual nature could make it a versatile compound for different applications in chemical processes.

Interesting facts

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

4-(Dimethylamino)-2-(1-naphthyl)butanenitrile, often abbreviated as DMAN, is a fascinating compound in the field of organic chemistry. Here are some intriguing aspects about this compound:

  • Structural Complexity: DMAN possesses a unique structure that includes a dimethylamino group attached to a naphthyl butanenitrile. This combination can influence its reactivity and properties dramatically.
  • Applications: Due to its chemical structure, DMAN has applications in various fields, including organic synthesis and as a potential building block in pharmaceuticals.
  • Fluorescent Properties: Some derivatives of compounds similar to DMAN exhibit fluorescence. This property can be exploited in dye research and as indicators in biochemical assays.
  • Research Potential: The presence of the dimethylamino moiety makes DMAN a candidate for further research in medicinal chemistry, especially in targeting specific pathways in disease mechanisms.
  • Importance of Naphthalene: The incorporation of a naphthyl ring contributes to its electronic properties, lending insights into the **π-π stacks** and enhancing the stability of the compound.

As an ever-evolving area of study, organic compounds like DMAN showcase how even the most intricate of structures contribute to modern chemistry. Moreover, their potential applications can lead to breakthroughs in various scientific arenas.

In the words of chemist Linus Pauling, “The best way to have a good idea is to have lots of ideas.” Exploring compounds like 4-(dimethylamino)-2-(1-naphthyl)butanenitrile encourages creative thinking and innovation in the field!

Synonyms
2809-54-3
BRN 2119878
alpha-(2-(Dimethylamino)ethyl)-1-naphthaleneacetonitrile
1-NAPHTHALENEACETONITRILE, alpha-(2-(DIMETHYLAMINO)ETHYL)-
SCHEMBL9735740
DTXSID10950825
XWDJWSFNFKEVBR-UHFFFAOYSA-N
4-Dimethylamino-2-(naphth-1-yl)butyronitrile
4-(dimethylamino)-2-(1-naphthyl)butanenitrile
4-(dimethylamino)-2-(naphthalen-1-yl)butanenitrile