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Isobornyl Ethoxypropanoate

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Identification
Molecular formula
C15H28O3
CAS number
68797-92-0
IUPAC name
(2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate
State
State

At room temperature, Isobornyl Ethoxypropanoate is a liquid, making it suitable for applications where a non-solid compound is required.

Melting point (Celsius)
-25.00
Melting point (Kelvin)
248.00
Boiling point (Celsius)
281.00
Boiling point (Kelvin)
554.00
General information
Molecular weight
240.36g/mol
Molar mass
240.3600g/mol
Density
0.9240g/cm3
Appearence

The compound appears as a clear, colorless liquid.

Comment on solubility

Solubility of (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate

The solubility of (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate is a topic of interest due to its unique structure, which influences its behavior in various solvents. Here are some key points regarding its solubility:

  • Polarity: The presence of both hydrocarbon regions and an ethoxy group contributes to a mixed polarity, making it more soluble in organic solvents.
  • Alcohol and Ether Solubility: This compound is likely to show good solubility in polar aprotic solvents like ethers and alcohols due to hydrogen bonding capabilities.
  • Hydrocarbon Solubility: It is expected to perform well in non-polar solvents, thanks to its cyclohexyl and isopropyl groups.
  • Temperature Effects: Increased temperatures may enhance solubility in organic solvents, which is a common trend in organic compounds.

In summary, while specific solubility values can vary based on conditions, it can be asserted that (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate is generally soluble in a range of organic solvents, making it versatile for different applications.

Interesting facts

Interesting Facts about (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate

(2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate is a fascinating compound with unique properties and applications. Here are some intriguing insights into this multi-faceted molecule:

  • Versatile Usage: This compound is often utilized in various industrial applications, particularly in the production of fragrances and flavorings. Its pleasing olfactory characteristics make it a valuable ingredient in the cosmetic industry.
  • Potential Benefits: Research indicates that compounds similar to (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate can exhibit beneficial properties, such as acting as solvents, emulsifiers, and plasticizers in various formulations.
  • Chemistry Behind the Name: The complex nomenclature reflects its intricate structure, showcasing both cycloalkyl and ester functionalities. The presence of an ethoxy group highlights its potential for further chemical derivatization.
  • Green Chemistry: This compound aligns with principles of green chemistry as it is derived from natural sources and can contribute to the development of sustainable products.
  • Scientific Exploration: Being at the intersection of organic and industrial chemistry, (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate serves as an excellent subject for students and researchers to explore concepts such as reactivity, stability, and synthesis in organic chemistry.

Understanding such compounds can provide valuable insights into the design and production of effective materials in science and industry. Exploring pathways and chemical reactions involving (2-isopropyl-5-methyl-cyclohexyl) 3-ethoxypropanoate opens up a treasure trove of learning opportunities for budding chemists.

In the words of a famous chemist, "The world is not only more complex than we think, but more complex than we can think." This sentiment rings especially true as we delve into the intriguing world of chemical compounds!

Synonyms
17162-28-6
(5-methyl-2-propan-2-ylcyclohexyl)3-ethoxypropanoate
DTXSID60938012
GIIWJGBQXMKNEH-UHFFFAOYSA-N
5-Methyl-2-(propan-2-yl)cyclohexyl 3-ethoxypropanoate