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Carvone

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Identification
Molecular formula
C10H14O
CAS number
99-49-0
IUPAC name
2-isopropenyl-5-methyl-cyclohexanone
State
State

At room temperature, carvone is a liquid.

Melting point (Celsius)
-31.00
Melting point (Kelvin)
242.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
150.22g/mol
Molar mass
150.2220g/mol
Density
0.9650g/cm3
Appearence

Carvone is a colorless to pale yellow liquid with a characteristic sweet, mint-like aroma. It is commonly found in essential oils such as caraway and dill.

Comment on solubility

Solubility of 2-isopropenyl-5-methyl-cyclohexanone

The solubility of 2-isopropenyl-5-methyl-cyclohexanone in various solvents can provide valuable insights into its chemical behavior and potential applications. This compound is primarily classified within the category of cyclic ketones, which often exhibit unique solubility characteristics.

In general, the solubility of 2-isopropenyl-5-methyl-cyclohexanone can be influenced by several factors:

  • Polarity: Being a ketone, this compound displays moderate polarity, allowing it to dissolve in both polar and non-polar solvents to some extent.
  • Hydrogen Bonding: The presence of a carbonyl group can engage in hydrogen bonding with solvents that can donate hydrogen bonds, enhancing solubility in alcohols and some polar aprotic solvents.
  • Molecular Structure: The bulky isopropenyl group and the methyl substitution may hinder solubility in highly polar solvents but enhance solubility in non-polar organic solvents.

While specific solubility data might be limited, it can be anticipated that:

  • 2-isopropenyl-5-methyl-cyclohexanone is likely to be soluble in organic solvents such as ethanol, acetone, and benzene.
  • Its solubility in water is likely to be low, due to its hydrophobic cyclohexane ring and bulky substituents.

Understanding the solubility of 2-isopropenyl-5-methyl-cyclohexanone is crucial for its application in various fields, such as synthetic organic chemistry and fragrance formulation.

In conclusion, the solubility profile of this compound emphasizes the interplay between its molecular features and solvent properties, thus pointing to its potential applications. Always conduct experiments under controlled conditions to confirm solubility behavior.

Interesting facts

Interesting Facts About 2-isopropenyl-5-methyl-cyclohexanone

2-isopropenyl-5-methyl-cyclohexanone is a fascinating compound with unique structural and chemical properties that make it a subject of interest among chemists. Here are some noteworthy aspects of this compound:

  • Structural Characteristics: This compound features a cyclohexanone ring, which is a six-membered carbon ring with a ketone functional group. The presence of the isopropenyl group adds a level of complexity, allowing for interesting reactivity patterns.
  • Synthesis Importance: The synthetic pathways leading to 2-isopropenyl-5-methyl-cyclohexanone often involve aldol condensation or Michael addition reactions, which are essential techniques in organic chemistry for constructing complex molecules.
  • Applications in Industry: This compound has potential applications in the fragrance industry due to the pleasant scents associated with its structure. It can also serve as an intermediate in the synthesis of more complex organic molecules.
  • Biological Activities: Some studies have suggested that derivatives of cyclohexanone display various biological activities, such as antimicrobial and anti-inflammatory properties, making it an area of interest in medicinal chemistry.
  • Research Opportunities: The unique configuration of this compound invites research into its physical and chemical properties, including reactivity and stability under various conditions. This can pave the way for the discovery of new reaction mechanisms.
  • Graphical Representations: Representing the structure of 2-isopropenyl-5-methyl-cyclohexanone using 3D molecular modeling can help visual learners understand the spatial arrangement of atoms and the significance of stereochemistry in its reactivity.

The multifaceted nature of 2-isopropenyl-5-methyl-cyclohexanone not only enriches our understanding of organic compounds but also highlights the importance of continued exploration in the field of chemistry. As the saying goes in the scientific community, "Every compound tells a story; it's up to us to decipher it."

Synonyms
529-00-0
Cyclohexanone, 5-methyl-2-(1-methylethenyl)-
DTXSID40865498
RefChem:1082602
DTXCID00813899
p-menth-8-en-3-one
5-methyl-2-(prop-1-en-2-yl)cyclohexan-1-one
1-Methyl-4-isopropenyl-3-cyclohexanone
2-Isopropenyl-5-methylcyclohexanone #
(-)-trans-Isopulegone
SCHEMBL727954
CHEBI:37046
(-)-trans-p-Menth-8-en-3-one
SAA88243
AKOS015907574
Cyclohexanone, 2-isopropylideno-5-methyl-
5-methyl-2-(prop-1-en-2-yl)cyclohexanone
NS00096354
EN300-2968121
Q27117020
(2R-trans)-5-methyl-2-(1-methylethenyl)-cyclohexanone