Interesting facts
Exploring 1-(Cyclohexen-1-yl)ethanone
1-(Cyclohexen-1-yl)ethanone is a fascinating organic compound that plays a notable role in various domains of chemistry, especially in the synthesis of complex molecules. Here are some intriguing aspects about this compound:
- Functional Group: As a ketone, this compound features the carbonyl group (C=O), which is vital in many biochemical processes and industrial applications, including the manufacture of fragrances, pharmaceuticals, and agrochemicals.
- Structural Diversity: The cyclohexenyl group introduces interesting stereochemistry and reactivity characteristics. This structural variance can lead to unique reactivity patterns compared to simple ketones.
- Reactivity: Ketones are generally known for their ability to undergo nucleophilic addition reactions. The presence of the cyclohexenyl group may influence how the molecule reacts with other compounds, making it a useful intermediate in organic synthesis.
- Application in Synthesis: This compound can be utilized in creating more complex structures, including natural products and pharmaceuticals, thanks to its reactive sites that can participate in various chemical reactions.
- Research Interest: The compound is of particular interest in organic synthesis research, including studies focused on reaction mechanisms and the development of new synthetic methods guided by its unique structure.
In summary, 1-(cyclohexen-1-yl)ethanone is more than just a simple ketone; it serves as a gateway to understanding the intricacies and potential of organic compounds in modern chemistry. Its structural elements, reactivity, and applications make it a significant player in both academic and industrial settings.
Synonyms
1-Acetyl-1-cyclohexene
932-66-1
1-Acetylcyclohexene
Ethanone, 1-(1-cyclohexen-1-yl)-
Methyl 1-cyclohexenyl ketone
Ketone, 1-cyclohexen-1-yl methyl
1-Cyclohexen-1-yl methyl ketone
Cyclohex-1-enylmethylketone
1-(1-CYCLOHEXEN-1-YL)ETHANONE
7539U6WQBL
EINECS 213-256-5
NSC-12216
1-cyclohexenyl methyl ketone
1-cyclohex-1-en-1-ylethanone
1-CYCLOHEXEN-1-YLETHANONE
NSC 12216
1Acetyl1cyclohexene
Cyclohex1enylmethylketone
213-256-5
inchi=1/c8h12o/c1-7(9)8-5-3-2-4-6-8/h5h,2-4,6h2,1h
1-(cyclohex-1-en-1-yl)ethanone
1-(cyclohexen-1-yl)ethanone
1-(cyclohex-1-en-1-yl)ethan-1-one
1-cyclohex-1-enyl-ethanone
1-(1-cyclohexenyl)-ethanone
MFCD00001547
88449-93-8
UNII-7539U6WQBL
Ethanone, 1-(cyclohexen-1-yl)-
cyclohexenyl-ethanone
1-acetyl-cyclohexene
1-acetyl1-cyclohexene
SCHEMBL310711
ghl.PD_Mitscher_leg0.1062
1-Acetyl-1-cyclohexene, 97%
CHEMBL5279035
DTXSID50862478
1-(1-Cyclohexen-1-yl)ethanone #
NSC12216
AKOS009158669
BS-51056
SY012913
DB-057388
CS-0155078
NS00042241
E76703
EN300-108706
Q27266337
Solubility of 1-(cyclohexen-1-yl)ethanone
1-(cyclohexen-1-yl)ethanone is a fascinating compound with distinct solubility characteristics. This molecule's solubility can be influenced by various factors:
In general, it shows limited solubility in water due to the hydrophobic cyclohexene ring, which can hinder interaction with water molecules. One might say that:
To summarize, 1-(cyclohexen-1-yl)ethanone exhibits solubility in organic solvents while facing challenges in polar environments such as water. Therefore, understanding these dynamics is crucial for practical usage in various chemical processes.