Camphor
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- Molecular formula
- C10H16O
- CAS Number
- 76-22-2
- IUPAC Name
- 1,3,3,7-tetramethylnorbornan-2-one
- Molecular Weight
- 152.24g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.9920g/cm3
- Synonyms
- 15404-57-6
Identification
Interesting facts
Interesting Facts about 1,3,3,7-Tetramethylnorbornan-2-one
1,3,3,7-Tetramethylnorbornan-2-one is a fascinating compound in the field of organic chemistry, especially for its unique structural characteristics and potential applications. Here are some intriguing aspects of this compound:
- Structural Beauty: The molecule is a derivative of norbornane, showcasing a bicyclic structure that is both robust and versatile. The presence of four methyl groups at positions 1, 3, and 7 adds to its complexity and interesting sterics.
- Synthesis Potential: This compound can be synthesized through various methods, including the photochemical degradation of derivatives or through multi-step synthetic pathways. Its synthesis provides ample opportunities for students to explore advanced organic reactions.
- Applications: 1,3,3,7-Tetramethylnorbornan-2-one is of interest in the synthesis of other organic compounds, potentially serving as a building block in the pharmaceutical and agrochemical industries.
- Chirality and Isomerism: The unique arrangement of its substituents offers a rich discussion on chirality and stereochemistry, making it an excellent study case for students interested in these concepts.
- Intriguing Reactivity: As a ketone, its chemical reactivity is quite interesting, allowing for various reactions including nucleophilic additions. This makes it a subject of interest for research in reaction mechanisms.
Through its structural features, synthetic pathways, and applications, 1,3,3,7-tetramethylnorbornan-2-one embodies the intersection of science and creativity, inspiring new ideas and developments in the chemical world. As a compound with multiple potential applications, it certainly deserves a prominent place in the study of organic chemistry.