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Cumyl alcohol

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Identification
Molecular formula
C12H18O
CAS number
617-94-7
IUPAC name
2-(4-isopropylphenyl)propan-2-ol
State
State

At room temperature, Cumyl alcohol is typically in a solid crystalline state or may appear as a liquid depending on the specific room conditions. It has a relatively low melting point for a solid organic compound, which means slight increases in temperature could result in it being a liquid.

Melting point (Celsius)
23.50
Melting point (Kelvin)
296.65
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
164.26g/mol
Molar mass
164.2580g/mol
Density
0.9702g/cm3
Appearence

Cumyl alcohol appears as a colorless to pale yellow liquid. It may also appear as a crystalline solid under certain conditions. It has a distinct aromatic odor which is characteristic of this compound.

Comment on solubility

Solubility of 2-(4-isopropylphenyl)propan-2-ol

The solubility of 2-(4-isopropylphenyl)propan-2-ol, a secondary alcohol, is influenced by several factors. Here are some key points to consider:

  • Polar vs. Non-polar: 2-(4-isopropylphenyl)propan-2-ol contains both hydrophobic phenyl groups and a polar hydroxyl group. This dual nature suggests that it may exhibit moderate solubility in polar solvents such as water due to hydrogen bonding, while also being soluble in non-polar organic solvents.
  • Temperature Dependency: The solubility can change with temperature. Typically, solubility increases with temperature for organic compounds, which may enhance its solvation in organic solvents.
  • Concentration Effects: At higher concentrations, the solubility may diminish due to interaction with itself or precipitation; thus, it is crucial to consider the conditions under which it is being tested.
  • pH Influence: The pH of the solution could also play a role, particularly if the compound undergoes ionization in extreme conditions, potentially affecting its solubility.

In summary, while 2-(4-isopropylphenyl)propan-2-ol is expected to have moderate solubility in polar solvents, its solubility profile is multifaceted and highly dependent on external conditions such as solvent choice, temperature, and concentration. As such, it remains essential to evaluate experimental solubility under specific conditions for accurate understanding.

Interesting facts

Interesting Facts About 2-(4-isopropylphenyl)propan-2-ol

2-(4-isopropylphenyl)propan-2-ol, commonly referred to as isopropyl-linked phenylpropanol, is a fascinating compound that exhibits interesting characteristics and applications. Here are some notable points about this compound:

  • Synthesis Role: It can be synthesized through a series of alkylation reactions, showcasing the versatility of organic synthesis methods.
  • Chirality: The compound contains a chiral center, which means it exists in enantiomeric forms. This property is crucial in fields like pharmaceuticals, where different enantiomers can have significantly different biological effects.
  • Psychoactive Potential: Similar compounds in its class have been explored for their effects on the central nervous system, raising interest in their potential as therapeutic agents.
  • Structure-Activity Relationship (SAR): The structure of 2-(4-isopropylphenyl)propan-2-ol provides a rich basis for understanding how structural changes influence activity, which is essential in drug design.
  • Industrial Applications: It may serve as a precursor in the production of various chemicals, reflecting its importance in industrial chemistry.

As a compound with intriguing structural features and potential applications, 2-(4-isopropylphenyl)propan-2-ol embodies the exciting possibilities of organic chemistry. Researchers continue to explore its properties and applications, bridging gaps between fundamental science and practical use.

In the words of a noted chemist, "The beauty of chemistry lies in its ability to transform simple building blocks into complex, life-changing substances."

Synonyms
alpha-Hydroxy-alpha'-(tert-butylperoxy)diisopropylbenzene
Benzenemethanol, (1-((1,1-dimethylethyl)dioxy)-1-methylethyl)-alpha,alpha-dimethyl-
benzenemethanol, [1-[(1,1-dimethylethyl)dioxy]-1-methylethyl]-.alpha.,.alpha.-dimethyl-
3445-42-9
p-Hydroxydiisopropylbenzene
2-(4-propan-2-ylphenyl)propan-2-ol
2-[4-(propan-2-yl)phenyl]propan-2-ol
p-Oxidiisopropylbenzene
2-(4-isopropylphenyl)propan-2-ol
2-(4-iso-propylphenyl)-2-propanol
Benzenemethanol, alpha,alpha-dimethyl-4-(1-methylethyl)-
4-Isopropyl-alpha,alpha-dimethylbenzyl alcohol
NSC-5106
2-(4-isopropyl-phenyl)-2-propanol
Benzyl alcohol, .alpha.,.alpha.-dimethyl-p-isopropyl-
Benzenemethanol, .alpha.,.alpha.-dimethyl-4-(1-methylethyl)-
NSC 5106
BRN 1936571
4-Isopropyl-|A,|A-dimethylbenzyl alcohol
alpha,alpha-Dimethyl-p-isopropylbenzyl alcohol
NSC5106
2-(4-Isopropylphenyl)-2-propanol
GH36EQ56EZ
SCHEMBL565578
BENZYL ALCOHOL, alpha,alpha-DIMETHYL-p-ISOPROPYL-
DTXSID30955993
CHEBI:189408
(p-Isopropylphenyl)dimethylcarbinol
2-(p-Isopropylphenyl)-2-propanol
(4-Isopropylphenyl)dimethylcarbinol
DAA44542
AKOS012095222
4-Isopropyl-?,?-dimethylbenzyl alcohol
DB-218948
CS-0233752
D87817
EN300-135882
.alpha.,.alpha.-Dimethyl-p-isopropylbenzyl alcohol
Benzyl alcohol, p-isopropyl-alpha,alpha-dimethyl-
alpha,alpha-Dimethyl-4-(1-methylethyl)benzenemethanol