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Campholenic Ketone

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Identification
Molecular formula
C11H20O
CAS number
77-68-9
IUPAC name
4-(1,1-dimethylpropyl)cyclohexanone
State
State

At room temperature, Campholenic Ketone is in a liquid state. It is relatively volatile, which contributes to its noticeable odor.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
203.00
Boiling point (Kelvin)
476.15
General information
Molecular weight
168.28g/mol
Molar mass
168.2760g/mol
Density
0.9158g/cm3
Appearence

Campholenic Ketone typically appears as a colorless liquid. It possesses a camphor-like aroma which is characteristic due to its structure derived from camphor.

Comment on solubility

Solubility of 4-(1,1-dimethylpropyl)cyclohexanone

The solubility of 4-(1,1-dimethylpropyl)cyclohexanone, a cyclohexanone derivative, presents interesting characteristics due to its molecular structure and functional groups. Being a ketone, it often features moderate solubility in a range of solvents:

  • Polar Solvents: This compound is likely to show some solubility in polar solvents such as water due to its carbonyl (C=O) group, which can engage in hydrogen bonding, though it may not be highly soluble.
  • Non-Polar Solvents: It is expected to be more soluble in non-polar solvents such as hexane or benzene because of the hydrophobic regions contributed by the alkyl groups attached to the cyclohexanone ring.
  • Temperature Dependence: Its solubility may also vary with temperature; generally, higher temperatures can increase solubility in both polar and non-polar solvents.

Analyzing solubility entails considering several factors:

  1. Molecular Weight: The relatively moderate molecular weight may facilitate easier dispersion in various solvents.
  2. Structural Features: Its bulky alkyl substituents could hinder solvation in certain environments, especially polar ones.
  3. Interactions: The ability of the carbonyl group to participate in hydrogen bonding will enhance solubility in specific circumstances.

In summary, while 4-(1,1-dimethylpropyl)cyclohexanone's solubility is influenced by the balance between its polar functional group and non-polar hydrocarbon regions, its behavior in solutions remains an area of interesting research for chemists.

Interesting facts

Interesting Facts about 4-(1,1-dimethylpropyl)cyclohexanone

4-(1,1-dimethylpropyl)cyclohexanone is an intriguing compound with unique properties and applications that make it a subject of interest in both academic and industrial settings. Here are some fascinating insights:

  • Structure and Stability: The molecule features a cyclohexanone ring, which is a six-membered carbon ring with a ketone functional group. This structure imparts a degree of stability, making it an important building block in organic synthesis.
  • Origin of Name: The “4-(1,1-dimethylpropyl)” part of the name reflects the presence of a branched alkyl group. This substitution significantly affects the physical and chemical properties compared to its simpler derivatives.
  • Applications: Compounds like 4-(1,1-dimethylpropyl)cyclohexanone are often used in the synthesis of fragrances and flavoring compounds. Their unique molecular structure allows them to interact with biological systems in interesting ways.
  • Scientific Exploration: Due to its distinctive characteristics, it has been a topic of numerous studies aimed at understanding its reactivity and interactions, particularly in organic chemistry and materials science.
  • Environmental Impact: Like many organic compounds, it is essential to consider the environmental ramifications of its production and use. Research is ongoing to assess its safety and ecological effects.

In conclusion, 4-(1,1-dimethylpropyl)cyclohexanone exemplifies the complexity and variety within organic chemistry. As scientists continue to explore its potential, it remains a pivotal component in various chemical research and applications.

Synonyms
16587-71-6
4-tert-Pentylcyclohexanone
4-tert-Amylcyclohexanone
Cyclohexanone, 4-(1,1-dimethylpropyl)-
4-(1,1-Dimethylpropyl)cyclohexanone
Orivone
CYCLOHEXANONE, 4-tert-PENTYL-
NSC 21167
4-(tert-Pentyl)-cyclohexanone
EINECS 240-642-0
isopentylcyclohexanone
BRN 2240475
DTXSID4047127
AI3-39162
4-Isopentylcyclohexanone
5380BWU79X
NSC-21167
DTXCID2027127
4-07-00-00096 (Beilstein Handbook Reference)
ISOPENTYLCYCLOHEXANONE [INCI]
240-642-0
4-(tert-Pentyl)cyclohexanone
4-(2-methylbutan-2-yl)cyclohexan-1-one
MFCD00013798
UNII-5380BWU79X
NSC21167
p-tert-Amylcyclohexanone
4-tert-pentyl-cyclohexanone
SCHEMBL112039
CHEMBL3182470
SCHEMBL27902476
Cyclohexanone,1-dimethylpropyl)-
DCSKAMGZSIRJAQ-UHFFFAOYSA-
WLN: L6VTJ DX2&1&1
RAA58771
Tox21_302460
4-(2-Methyl-sec-butyl)cyclohexanone
4-(2-Methyl-2-butanyl)cyclohexanone
AKOS000119101
4-(TERT.-PENTYL)-CYCLOHEXANONE
4-(1,1-dimethylpropyl)cyclohexan-1-one
NCGC00256850-01
AS-63850
CAS-16587-71-6
DB-043630
CS-0207042
NS00011976
ST50406892
EN300-19066
F71288
Q27261076
Z104472532
InChI=1/C11H20O/c1-4-11(2,3)9-5-7-10(12)8-6-9/h9H,4-8H2,1-3H3