Leaf Alcohol

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Identification

Molecular formula
C8H16O
CAS Number
3391-86-4
IUPAC Name
oct-3-en-1-ol
Molecular Weight
128.21g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.8476g/cm3
Synonyms
3-OCTEN-1-OL
Interesting facts

Exploring the Chemistry of Oct-3-en-1-ol

Oct-3-en-1-ol is a fascinating organic compound that belongs to the family of alkenols, which are characterized by the presence of both a double bond and a hydroxyl (-OH) functional group. This unique structure gives it intriguing properties and applications.

Key Characteristics

  • Source: Oct-3-en-1-ol can be found naturally in several essential oils and is often associated with a variety of scents.
  • Reactivity: Its double bond makes it susceptible to various types of reactions, such as hydrogenation and oxidation, thereby participating in significant organic transformations.
  • Versatility: This compound can serve as an important intermediate in the synthesis of more complex molecules, showcasing its utility in organic chemistry.

Applications & Uses

Oct-3-en-1-ol is notable for its diverse applications:

  • Fragrance Industry: Its pleasant aroma allows it to be utilized in perfumes and flavorings, adding unique notes to various products.
  • Pharmaceuticals: Several studies have explored its potential for use in medicinal chemistry, where it can act as a building block for drug development.
  • Agricultural Chemistry: Some research has demonstrated its potential in formulations for plant protection, acting as a bioactive agent.

Quote from a Chemist

As one chemist aptly put it, "Oct-3-en-1-ol stands at the crossroads of organic synthesis and natural product chemistry, merging functionality with elegance."

In summary, Oct-3-en-1-ol is more than just an organic compound; its diverse applications and reactivity make it a noteworthy subject of study in modern chemistry.

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