Camphene (ester of propanoic acid)
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- Molecular formula
- C14H24O2
- CAS Number
- 38353-09-4
- IUPAC Name
- (4,7,7-trimethylnorbornan-2-yl) propanoate
- Molecular Weight
- 208.35g/mol
- Melting Point
- means that it does not solidify under normal room conditions. It is non-aqueous and may separate from water if mixed. The volatility is typical of esters, contributing to the compound's odor.
- Boiling Point
- (Celsius)
- Density
- 0.8880g/cm3
- Synonyms
- SCHEMBL759346
Identification
Interesting facts
Interesting Facts about (4,7,7-trimethylnorbornan-2-yl) propanoate
(4,7,7-trimethylnorbornan-2-yl) propanoate is a fascinating compound that blends the intriguing structural characteristics of norbornane derivatives with the functionalities of ester chemistry. Here are some notable aspects of this compound:
- Unique Structure: The compound features a bicyclic structure, which contributes to its interesting conformational dynamics. This bicyclic framework is essential in many natural products and pharmaceuticals.
- Applications: As an ester, it possesses potential uses in the fragrance and flavor industry. Esters are often associated with pleasant scents and sweet flavors, making them desirable in various consumer products.
- Synthetic Utility: The synthesis of (4,7,7-trimethylnorbornan-2-yl) propanoate often involves sophisticated organic reactions, showcasing the versatility of organic methodologies. Its formation elucidates the significance of sterics and electronic effects in organic synthesis.
- Chirality: This compound potentially exhibits chiral properties due to its complex structure, allowing for interesting studies in asymmetric synthesis and the behavior of chiral molecules in biological systems.
- Research Potential: Scientists may probe its properties to discover novel reactivity patterns or biological activities, making it an appealing compound for chemical research.
As you dive into the world of (4,7,7-trimethylnorbornan-2-yl) propanoate, remember that every compound tells a story of nature, structure, and function. Keep exploring!