Camphorquinone

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Identification

Molecular formula
C10H14O2
CAS Number
10373-78-1
IUPAC Name
3-benzylidene-1,7,7-trimethyl-norbornan-2-one
Molecular Weight
204.29g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0545g/cm3
Appearance
characterized by its bright yellow color and is typically encountered in powder or crystalline form.
Synonyms
15087-24-8
Interesting facts

Interesting Facts about 3-Benzylidene-1,7,7-trimethyl-norbornan-2-one

3-Benzylidene-1,7,7-trimethyl-norbornan-2-one is a fascinating compound that exhibits unique structural characteristics and potential applications. This compound belongs to the class of norbornanones, which are cyclic ketones that feature intriguing ring structures. Here are some interesting points:

  • Structural Diversity: The compound's structure showcases a bicyclic framework, which contributes to its unique spatial arrangement. The presence of both a benzylidene and a ketone moiety enhances its reactivity and lends itself to diverse chemical reactions.
  • Regioselectivity: The specific placement of groups in the norbornanone makes this compound an excellent candidate for studying regioselectivity in chemical transformations, offering insights into reaction pathways.
  • Applications in Synthesis: Due to its reactive functional groups, this compound can be utilized as an intermediate in organic synthesis, particularly in the design and creation of more complex natural products.
  • Potential Biological Activity: Compounds related to norbornanones have been explored for various biological activities, including antimicrobial and anti-inflammatory properties, making them of interest in medicinal chemistry.
  • Research Opportunities: This compound opens the door to a variety of experimental studies, providing opportunities for chemistry students and researchers to delve into synthesis methods, reaction mechanisms, and practical applications.
  • Chirality: The presence of multiple chiral centers in the molecule creates opportunities for enantiomeric studies, which are crucial for understanding the effects of chirality in pharmacology.

The study of 3-benzylidene-1,7,7-trimethyl-norbornan-2-one is not only rich in organic chemistry applications but also offers avenues for innovation in materials science and drug development. As one dives into research involving this compound, one may uncover novel reactions and mechanisms that could contribute significantly to the field.

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