Sulcatone
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- Molecular formula
- C9H16O
- CAS Number
- 110-93-0
- IUPAC Name
- 2,6-dimethylhept-2-en-4-one
- Molecular Weight
- 140.23g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.8324g/cm3
- Synonyms
- 2, 6-DIMETHYL-2-HEPTEN-4-ONE
Identification
Interesting facts
Interesting Facts about 2,6-Dimethylhept-2-en-4-one
2,6-Dimethylhept-2-en-4-one is a fascinating organic compound that showcases the diversity found within ketones. Here are some intriguing aspects of this compound:
- Structural Characteristics: This compound features a unique structure that includes a double bond, which classifies it as an unsaturated ketone. The presence of two methyl groups on the sixth and second carbon atoms adds to its complexity.
- Synthesis: 2,6-Dimethylhept-2-en-4-one can be synthesized through various methods. One common approach involves the aldol condensation, allowing chemists to create this compound with precision. The reaction conditions play a crucial role in determining the yield and purity of the product.
- Reactivity: As with other ketones, this compound exhibits fascinating reactivity. It can undergo nucleophilic addition reactions, making it valuable in organic synthesis for creating more complex molecules.
- Applications: Compounds like 2,6-dimethylhept-2-en-4-one can be used in the fragrance and flavor industry due to their appealing aromatic properties, serving as important intermediates in scent production.
- Biological Significance: The study of such compounds often leads to insights into their biological activity. Some ketones are known to exhibit antimicrobial and anti-inflammatory properties, highlighting their potential in pharmaceutical applications.
In summary, 2,6-dimethylhept-2-en-4-one is not just another ketone; it is a compound that stands at the intersection of organic chemistry and practical application. As a chemistry student or enthusiast, understanding its structure, synthesis, and significance can deepen your appreciation for the complexities and utilities of chemical compounds.