Nerol

ADVERTISEMENT

Identification

Molecular formula
C10H18O
CAS Number
106-25-2
IUPAC Name
nona-2,6-dien-1-ol
Molecular Weight
154.25g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.8774g/cm3
Synonyms
2, 6-Nonadien-1-ol
Interesting facts

Interesting Facts About Nona-2,6-dien-1-ol

Nona-2,6-dien-1-ol, also known by its IUPAC name, is a fascinating compound that falls into the category of unsaturated alcohols. This compound is notable for several reasons:

  • Structure and Isomerism: Nona-2,6-dien-1-ol features a unique structure with two double bonds located at the 2nd and 6th carbon positions along a 9-carbon backbone. This configuration gives rise to interesting geometric isomers, influencing its reactivity and applications.
  • Natural Occurrence: Similar compounds are often found in nature, particularly in essential oils and plant extracts. Their presence contributes to the aromatic characteristics of numerous natural substances.
  • Synthesis Techniques: Chemists can synthesize nona-2,6-dien-1-ol through several methods, including dehydration of the corresponding diol or through selective catalytic hydrogenation processes. This variation in synthesis can lead to differences in purity and isomeric forms.
  • Applications: Nona-2,6-dien-1-ol's properties make it a valuable compound in the chemical industry for applications such as:
    • As an intermediate in the production of fragrances and flavorings, contributing to the pleasant scents of various products.
    • In pharmaceuticals, where its structural characteristics can lead to the development of new therapeutic agents.
  • Biological Activity: Some studies suggest that compounds like nona-2,6-dien-1-ol may possess biological activity, which could lead to potential health benefits or uses in medicinal chemistry.

In summary, nona-2,6-dien-1-ol is not just an ordinary alcohol; its unique structure, synthesis possibilities, and diverse applications make it a compound of interest for further study and exploration in both industrial and natural contexts.

ADVERTISEMENT