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.
Synonyms
15087-24-8
3-benzylidenebornan-2-one
DTXSID90864552
DTXCID40813055
benzylidene camphor
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-3-(phenylmethylene)-
3-benzylidene-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
1,7,7-trimethyl-3-(phenylmethylidene)bicyclo[2.2.1]heptan-2-one
(1S,4R)-3-[(E)-Benzylidene]-1,7,7-trimethylbicyclo[2.2.1]heptane-2-one
Maybridge1_002522
(E)-3-benzylidene camphor
SCHEMBL15171
DivK1c_001274
orb2695295
orb2695300
SCHEMBL5491883
BCP31898
AKOS016037998
1ST3415
CDS1_000234
NS00088708
(1S,3E,4R)-3-benzylidene-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
Solubility of 3-benzylidene-1,7,7-trimethyl-norbornan-2-one
The solubility of 3-benzylidene-1,7,7-trimethyl-norbornan-2-one can be quite intriguing due to its unique structural characteristics. Solubility often depends on several factors, including:
In the case of 3-benzylidene-1,7,7-trimethyl-norbornan-2-one, its relatively bulky and nonpolar structure suggests that it may have limited solubility in polar solvents like water. Instead, it is likely to be more soluble in:
As always, experimental validation is essential to determine the precise solubility characteristics, as theoretical predictions can vary. Understanding the solubility profile not only aids in practical applications but also opens the door to further chemical investigations.