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Perillyl alcohol

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Identification
Molecular formula
C10H16O
CAS number
536-59-4
IUPAC name
(4-isopropenylcyclohexen-1-yl)methanol
State
State

Perillyl alcohol is a liquid at room temperature.

Melting point (Celsius)
13.00
Melting point (Kelvin)
286.00
Boiling point (Celsius)
224.00
Boiling point (Kelvin)
497.00
General information
Molecular weight
152.24g/mol
Molar mass
152.2370g/mol
Density
0.9750g/cm3
Appearence

Perillyl alcohol is a colorless liquid with a characteristic citrus or floral odor. It is often found in essential oils of various plants, including peppermint, spearmint, and cherries.

Comment on solubility

Solubility of (4-isopropenylcyclohexen-1-yl)methanol

The solubility of (4-isopropenylcyclohexen-1-yl)methanol is a complex characteristic that can influence its application and behavior in various environments. This compound is expected to exhibit moderate solubility in organic solvents due to its hydrophobic cyclohexene ring structure combined with the polar hydroxyl group (-OH).

Factors influencing solubility include:

  • Molecular Structure: The presence of both a hydrophobic component and a hydrophilic alcohol functional group can lead to a balance in solubility properties.
  • Temperature: Increased temperature generally enhances solubility in organic solvents.
  • Solvent Polarity: Soluble in polar organic solvents like ethanol and acetone while showing limited solubility in water.

As a guideline, it is often stated that "like dissolves like," meaning that similar polarities of the solute and solvent can improve solubility prospects. Therefore, (4-isopropenylcyclohexen-1-yl)methanol’s solubility characteristics can be summarized as:

  • Good solubility: in organic solvents.
  • Poor solubility: in water.

Understanding these solubility parameters is crucial for applications such as formulation in pharmaceuticals, agrochemicals, or other industrial uses where solubility plays a significant role in efficacy and performance.

Interesting facts

Exploring (4-isopropenylcyclohexen-1-yl)methanol

(4-isopropenylcyclohexen-1-yl)methanol is a fascinating organic compound that has drawn interest in various fields, particularly in organic chemistry and medicinal chemistry due to its unique structural properties and potential applications. Here are some intriguing facts about this compound:

  • Structural Insights: The presence of both isopropenyl and cyclohexenyl groups within the molecule contributes to a rich array of chemical reactivity. This molecular architecture positions it as a target for synthetic chemists looking to explore ring-opening reactions and other transformations.
  • Natural Occurrence: Compounds related to (4-isopropenylcyclohexen-1-yl)methanol are often found in natural products. Some researchers have noted its resemblance to essential oils, suggesting a role in the aroma profiles of various plants.
  • Potential Applications: This compound holds promise in the fields of fragrance formulations and as a building block in medicinal chemistry. Its unique functional groups might contribute to various biological activities, sparking interest in drug discovery.
  • Synthetic Pathways: The synthesis of (4-isopropenylcyclohexen-1-yl)methanol can involve several methodologies, including the use of catalytic systems and multi-step organic reactions. This opens up discussions on eco-friendly synthesis and the use of renewable resources in its production.
  • Research Directions: Ongoing studies are aimed at understanding the interactions of (4-isopropenylcyclohexen-1-yl)methanol with biological systems. By elucidating its mechanisms and potential therapeutic effects, scientists hope to uncover new applications in treating various diseases.

In summary, (4-isopropenylcyclohexen-1-yl)methanol stands at the intersection of nature and synthetic innovation, making it a riveting subject of study in modern chemistry. As research continues to unfold, who knows what surprises this compound may hold for the scientific community?

Synonyms
PERILLYL ALCOHOL
536-59-4
Perillol
Isocarveol
p-Mentha-1,8-dien-7-ol
Hydrocumin alcohol
1-Cyclohexene-1-methanol, 4-(1-methylethenyl)-
Dihydrocuminyl alcohol
Iso-carveol
(4-(Prop-1-en-2-yl)cyclohex-1-en-1-yl)methanol
4-Isopropenylcyclohex-1-en-1-ylmethanol
4-Isopropenyl-cyclohex-1-ene-1-methanol
Dihydrocuminic alcohol
4-Isopropenyl-1-cyclohexene carbinol
(4-prop-1-en-2-ylcyclohexen-1-yl)methanol
FEMA No. 2664
1-Hydroxymethyl-4-isopropenyl-1-cyclohexene
4-(1-Methylethenyl)-1-cyclohexene-1-methanol
[4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol
CHEBI:15420
1,8-p-Menthadien-7-ol
Cyclohex-1-ene-1-methanol, 4-(1-methylethenyl)-
Para-mentha-1,8-dien-7-ol
Perillic alcohol
CHEMBL444711
319R5C7293
Dl-perillyl alcohol
NSC 641066
EINECS 208-639-9
(+/-)-PERILLYL ALCOHOL
perill alcohol
1-perillalcohol
CCRIS 8461
UNII-319R5C7293
dihydrocuminyl alcoholn
(-)-Perillyl alcohol?
Spectrum2_000838
Spectrum3_001974
BSPBio_003574
SCHEMBL296111
SPECTRUM1505297
SPBio_000795
DTXSID4052180
KBio3_002951
(-)-p-Mentha-1,8-diene-7-ol
HY-N7000
4-Isopropenyl-1-cyclohexene-methanol
BDBM50252404
CCG-40267
s3853
4-isopropenyl-cyclohex-1-enylmethanol
AKOS006227854
CS-W019441
FP70326
SB45076
SDCCGMLS-0066882.P001
NCGC00095297-01
NCGC00095297-02
NCGC00095297-03
AC-35110
SY110506
P-MENTHA-1,8-DIEN-7-OL [FHFI]
(4-Isopropenyl-1-cyclohexen-1-yl)methanol
DB-065484
DB-071728
NS00013107
EN300-97783
1-Hydroxymethyl-4-(1-methylvinyl)-cyclohexene
SR-05000002384
SR-05000002384-1
BRD-A13323580-001-03-0
BRD-A13323580-001-04-8
BRD-A13323580-001-05-5
Q15391928
(S)-[4-(1-Propen-2-yl)-1-cyclohexen-1-yl]methanol
Z1198147170
F9405E33-6136-4D27-A15E-C10CDC8C9AC4
(+/-)-1-CYCLOHEXENE-1-METHANOL, 4-(1-METHYLETHENYL)-