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Ethyl 6-cyanohexanoate

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Identification
Molecular formula
C9H15NO2
CAS number
16274-10-1
IUPAC name
ethyl 6-cyanohexanoate
State
State

At room temperature, ethyl 6-cyanohexanoate is a liquid.

Melting point (Celsius)
-34.00
Melting point (Kelvin)
239.00
Boiling point (Celsius)
270.00
Boiling point (Kelvin)
543.00
General information
Molecular weight
169.24g/mol
Molar mass
169.2370g/mol
Density
0.9785g/cm3
Appearence

Ethyl 6-cyanohexanoate typically appears as a colorless to pale yellow liquid. It has a characteristic ester odor.

Comment on solubility

Solubility of Ethyl 6-Cyanohexanoate

Ethyl 6-cyanohexanoate (C9H15NO2) exhibits interesting solubility characteristics that are important for its practical applications in various chemical processes.

Solubility in Different Solvents:

  • Polar Solvents: Ethyl 6-cyanohexanoate is generally soluble in polar solvents such as water, due to the presence of the cyano group and the ester functional group, which can engage in hydrogen bonding.
  • Non-Polar Solvents: It also demonstrates good solubility in non-polar solvents like hexane or toluene, which can be attributed to its aliphatic hydrocarbon chain.

The solubility behavior can be summarized as follows:

  • Moderate solubility in water
  • High solubility in organic solvents

It is noteworthy that the solubility of ethyl 6-cyanohexanoate can vary with temperature and concentration. As the temperature increases, solubility typically increases due to enhanced molecular motion.

In summary, the understanding of the solubility characteristics of ethyl 6-cyanohexanoate makes it a versatile compound in both chemical synthesis and industrial applications.

Interesting facts

Interesting Facts About Ethyl 6-Cyanohexanoate

Ethyl 6-cyanohexanoate is a versatile compound with a rich profile that resonates in both organic synthesis and biochemical applications. Here are some compelling aspects of this compound:

  • Functional Groups: Ethyl 6-cyanohexanoate contains both an ester and a nitrile functional group. This combination allows it to participate in various reactions, including nucleophilic additions and condensation reactions, making it an important intermediate in organic synthesis.
  • Synthetic Applications: This compound is commonly used in the manufacture of pharmaceuticals and agrochemicals. The presence of the cyano group enhances its utility in creating biologically active molecules.
  • Biological Relevance: Modified esters like ethyl 6-cyanohexanoate can interact with various biological systems. Research suggests that such compounds may exhibit interesting properties in drug design, especially for anti-inflammatory and anti-cancer therapies.
  • Reactivity: Due to the electrophilic nature of the carbon in the nitrile group, ethyl 6-cyanohexanoate is reactive towards nucleophiles, which makes it an excellent substrate for various chemical transformations, including hydrolysis and reduction.
  • Emerging Research: Ongoing studies are investigating the potential use of this compound in materials science, particularly in the development of new coatings and polymers due to its ability to impart unique physical properties when integrated with other materials.

In summary, ethyl 6-cyanohexanoate is not only a significant part of organic chemistry but also holds promise for innovative applications in drug discovery and materials science. Its wide range of reactivity and functional versatility highlights the intricate relationships between molecular structure and chemical properties.

Synonyms
Ethyl 6-cyanohexanoate
6-Cyanohexanoic acid, ethyl ester
HEXANOIC ACID, 6-CYANO-, ETHYL ESTER
NSC 92771
BRN 1762711
UNII-1A0611B745
NSC-92771
1A0611B745
DTXSID50143875
4-02-00-02006 (Beilstein Handbook Reference)
DTXCID1066366
10137-65-2
6-Cyanohexanoic acid ethyl ester
WLN: NC5VO2
SCHEMBL8657397
WPGIMPZMPWRYAI-UHFFFAOYSA-N
NSC92771
AKOS013618136
Q27252139