Leaf Alcohol
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- 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
Identification
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.