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Viminol

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Identification
Molecular formula
C9H17N
CAS number
126-91-0
IUPAC name
2-ethyl-3-(methylamino)hexanenitrile
State
State

At room temperature, it is a clear, colorless liquid.

Melting point (Celsius)
-51.00
Melting point (Kelvin)
222.15
Boiling point (Celsius)
235.00
Boiling point (Kelvin)
508.15
General information
Molecular weight
126.20g/mol
Molar mass
126.2010g/mol
Density
0.8936g/cm3
Appearence

The compound typically appears as a colorless liquid. It is an oily liquid with a faint odor.

Comment on solubility

Solubility of 2-ethyl-3-(methylamino)hexanenitrile

The solubility of 2-ethyl-3-(methylamino)hexanenitrile, a compound with the chemical formula C11H18N2, is influenced by its molecular structure and functional groups. Understanding its solubility is crucial for practical applications in synthesis and formulation. Here are some key points regarding its solubility:

  • Polar vs. Non-Polar Solubility: Due to the presence of the nitrile group (–C≡N) and the amine group (–NH2), this compound exhibits polar characteristics, which may enhance its solubility in polar solvents like water, but less so in non-polar solvents.
  • Hydrogen Bonding: The amine functional group allows for potential hydrogen bonding with polar solvents, increasing its solubility in such environments.
  • Chain Length and Branching: The carbon backbone of the molecule can impede complete solubility in water due to hydrophobic interactions from the long hydrocarbon chain.

In summary, 2-ethyl-3-(methylamino)hexanenitrile shows a balance between polar and non-polar properties, leading to variable solubility depending on the solvent used. Typically, it would be expected to have moderate solubility in polar solvents and limited solubility in non-polar solvents. Understanding these factors plays a vital role in its chemical behavior and application in various fields.

Interesting facts

Interesting Facts about 2-Ethyl-3-(methylamino)hexanenitrile

2-Ethyl-3-(methylamino)hexanenitrile is a fascinating compound that belongs to the family of nitriles. Its unique structure and properties make it significant in various fields, particularly in medicinal chemistry and organic synthesis.

Key Characteristics

  • Amine Group: The presence of the methylamino group in this compound enhances its reactivity, leading to various applications in pharmaceutical development.
  • Nitrile Group: The nitrile functional group lends itself to important synthetic transformations, turning this compound into a versatile building block in organic chemistry.
  • Chirality: 2-Ethyl-3-(methylamino)hexanenitrile can exist in stereoisomer forms, which may exhibit different biological activities, making stereochemistry an important consideration in its study.

Applications and Importance

This compound serves a range of applications:

  • It is often explored in the development of new pharmaceutical agents.
  • Its structural features allow it to act as a potential candidate for medications targeting neurological disorders.
  • Additionally, compounds with similar structures are studied for their effectiveness in anti-cancer therapies.

Did You Know?

This compound also exemplifies the ongoing research into the design of dual-action drugs that can address multiple health issues simultaneously. As scientists continue to explore its properties, we may yet uncover more groundbreaking uses for 2-ethyl-3-(methylamino)hexanenitrile. Remember, in the world of chemistry, the potential applications of a single compound can go beyond initial expectations, leading to significant discoveries!

In conclusion, 2-ethyl-3-(methylamino)hexanenitrile stands as an important compound in the realm of chemical research, illustrating the intricate connections between molecular structure and biological activity.

Synonyms
14339-29-8
2-ethyl-3-(methylamino)hexanenitrile
2-Ethyl-3-(N-methylamino)hexanonitrile
BRN 2349599
HEXANONITRILE, 2-ETHYL-3-(N-METHYLAMINO)-
DTXSID30931858