Geranyl acetate
- Molecular formula
- C12H20O2
- CAS Number
- 105-87-3
- IUPAC Name
- (2-isopropenyl-5-methyl-hex-4-enyl) acetate
- Molecular Weight
- 196.29g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.9080g/cm3
- Synonyms
- Lavandulyl acetate
Identification
Interesting Facts About (2-isopropenyl-5-methyl-hex-4-enyl) Acetate
(2-isopropenyl-5-methyl-hex-4-enyl) acetate, often referred to in research and industry for its unique structure and applications, presents a fascinating case for chemical study. Here are some noteworthy points regarding this compound:
- Derivative of Natural Compounds: This compound is a derivative of naturally occurring substances, often used in fragrances and flavorings, due to its pleasant aroma.
- Versatile Applications: Its structure allows it to be a precursor for various synthetic pathways, enhancing its utility in organic synthesis.
- Significant in Aromatherapy: (2-isopropenyl-5-methyl-hex-4-enyl) acetate is recognized for its potential roles in aromatherapy, contributing to the therapeutic qualities of essential oils.
Chemical Structure Insights
The compound's structure features a complex arrangement of carbon atoms, providing multiple points of reactivity. The presence of double bonds enhances its reactivity, making it suitable for various chemical transformations:
- Geometric Isomerism: The presence of double bonds allows for geometric isomerism, which can result in different physical and chemical properties.
- Functional Groups: Its acetate functional group plays a crucial role in its reactivity, particularly in esterification reactions.
Biological Implications
Research has shown that compounds like (2-isopropenyl-5-methyl-hex-4-enyl) acetate may possess biological activities, including:
- Antimicrobial Properties: Studies suggest that such compounds could have antimicrobial effects, making them of interest in pharmacology.
- Potential as a Repellent: There is ongoing investigation into its use as a natural repellent against pests, reflecting its ecological applications.
In summary, (2-isopropenyl-5-methyl-hex-4-enyl) acetate exemplifies the diverse roles chemical compounds can play in both nature and industry. Its unique structure makes it a compound of interest in research, with potential for various applications in fields such as aromatherapy, organic synthesis, and pharmacology.