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1-Cyclohexylethanone

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Identification
Molecular formula
C8H14O
CAS number
822-36-6
IUPAC name
1-cyclohexylethanone
State
State

At room temperature, 1-Cyclohexylethanone is in a liquid state. It is not highly viscous, allowing for ease of handling and use in various chemical applications.

Melting point (Celsius)
-42.50
Melting point (Kelvin)
230.65
Boiling point (Celsius)
208.00
Boiling point (Kelvin)
481.15
General information
Molecular weight
126.20g/mol
Molar mass
126.1960g/mol
Density
0.9377g/cm3
Appearence

1-Cyclohexylethanone is typically a colorless to pale yellow liquid. It has a slightly oily texture and may have a faint odor that is characteristic of ketones.

Comment on solubility

Solubility of 1-Cyclohexylethanone

1-Cyclohexylethanone, with the chemical formula C10H18O, presents interesting solubility characteristics that may intrigue both chemists and those studying organic compounds.

This compound is non-polar owing to its hydrocarbon structure with a ketone functional group. Consequently, it exhibits specific solubility behaviors:

  • Solubility in Organic Solvents: 1-Cyclohexylethanone is highly soluble in non-polar organic solvents such as hexane and toluene. This is due to the compatibility of its structure with these solvents.
  • Limited Water Solubility: On the flip side, water solubility is very limited. 1-Cyclohexylethanone does not mix well with water, aligning with the principle that "like dissolves like."
  • Implications: The solubility behavior influences applications in various industries, including fragrance and flavor manufacturing, where its solubility in organic solvents is advantageous.

In summary, while 1-cyclohexylethanone showcases excellent solubility in organic solvents, it remains largely insoluble in water, echoing the dynamics of organic chemistry.

Interesting facts

Interesting Facts about 1-Cyclohexylethanone

1-Cyclohexylethanone, often referred to in chemical discussions as a ketone, is an intriguing and versatile compound known for its applications in various fields. Here are some noteworthy points about this compound:

  • Structural Insights: The compound exhibits a unique structural configuration, containing both a cyclohexyl group and an ethanone moiety. This makes it an interesting example of cycloalkyl ketones.
  • Synthesis: Synthesis of 1-cyclohexylethanone can be achieved through various methods, including Friedel-Crafts acylation, which highlights its significance in organic synthesis and industrial applications.
  • Applications: Beyond its role in organic synthesis, this ketone is often utilized in the production of fragrances and flavorings due to its pleasant aroma. Additionally, it serves as a solvent in different chemical processes.
  • Reactivity: The presence of the carbonyl group in 1-cyclohexylethanone makes it reactive toward nucleophiles, contributing to its functionality in various chemical reactions, including nucleophilic addition and reduction processes.
  • Research Potential: The compound is of increasing interest in scientific research. Its unique properties may lead to discoveries in medicinal chemistry and materials science.

In summary, 1-cyclohexylethanone is more than just a simple ketone. Its structural attributes, reactivity, and application potential not only make it significant in the laboratory but also underline the broader relevance of carbonyl compounds in chemistry.

Synonyms
Cyclohexyl methyl ketone
1-Cyclohexylethan-1-one
Acetylcyclohexane
Ethanone, 1-cyclohexyl-
1-Acetylcyclohexane
Methyl cyclohexyl ketone
Cyclohexylethanone
Cyclohexane, acetyl-
Ketone, cyclohexyl methyl
Acetophenone, hexahydro-
Hexahydroacetophenone
NSC 16249
EINECS 212-517-0
UNII-U53404H6B8
NSC-16249
U53404H6B8
c-C6H11COCH3
DTXSID40231674
Ethanone, 1-cyclohexyl-(9CI)
DTXCID70154165
Ketone, cyclohexyl methyl (8CI)
rifkadjtwugdov-uhfffaoysa-n
1-Cyclohexylethanone
823-76-7
1-cyclohexyl-ethanone
MFCD00040418
Cyclohexylmethyl ketone
1-cyclohexylacetaldehyde
1-Cyclohexylethanone #
1-cyclohexyl-1-ethanone
CYCLOHEXYLMETHYLKETONE
SCHEMBL28019
CHEMBL5272368
SCHEMBL12891744
CHEBI:195514
AAA82376
NSC16249
AKOS005206946
CS-W007597
PS-4108
SB12754
SY013522
NS00038193
EN300-20257
P10040
Q27290697
F0001-2108