Interesting facts
Interesting Facts about 1,3,3-Trimethylnorbornan-2-one
The compound 1,3,3-trimethylnorbornan-2-one is a fascinating member of the norbornane family, exhibiting unique structural and chemical characteristics that make it an intriguing subject of study.
- Synthetic Pathways: This compound can be synthesized via complex organic reactions, often employing strategies such as the Diels-Alder reaction and subsequent functional group modifications. These techniques showcase the compound's structural versatility.
- Applications: 1,3,3-trimethylnorbornan-2-one is used in various applications, from material science to pharmaceuticals. Its structural framework is valuable in designing biologically active molecules.
- Chirality: The compound exhibits chirality, which is essential in the realm of chemistry. Chirality plays a critical role in the biological activity of compounds, influencing how they interact with biological systems.
- Insights into Isomers: The study of 1,3,3-trimethylnorbornan-2-one opens up fascinating discussions about isomerism—especially regarding the stereochemistry of its derivatives. Understanding how different isomers can influence properties is key in chemistry.
- Environmental Impact: Some research has explored the environmental impact of compounds similar to this one, particularly in terms of their role in atmospheric chemistry, which is essential for green chemistry initiatives.
As we delve further into the endless possibilities offered by 1,3,3-trimethylnorbornan-2-one, it becomes evident that compounds with a seemingly simple form can possess deep complexities that intrigue scientists and students alike. "Chemistry is not just about atoms and molecules; it's about connections and transformations!" This quote resonates deeply in the study of such dynamic compounds.
Synonyms
Fenchone
1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one
1195-79-5
dl-fenchone
alpha-Fenchone
Fenchon
1,3,3-Trimethyl-2-norbornanone
1,3,3-Trimethyl-2-norcamphanone
Bicyclo[2.2.1]heptan-2-one, 1,3,3-trimethyl-, (1S,4R)-
fenchan-2-one
NSC 8896
NSC 122687
CHEBI:4999
DTXSID9025324
Fenchon [German]
(.+/-.)-Fenchone
DTXCID305324
1,3,3-Trimethylbicyclo(2.2.1)heptan-2-one
EINECS 214-804-6
2,2,4-trimethylbicyclo[2.2.1]heptan-3-one
BRN 1861492
AI3-00736
Bicyclo(2.2.1)heptan-2-one, 1,3,3-trimethyl-, (1S,4R)-
2,2,4-trimethylbicyclo(2.2.1)heptan-3-one
FENCHONE [WHO-DD]
2-07-00-00093 (Beilstein Handbook Reference)
1,3,3Trimethylnorcamphor
1,3,3Trimethyl2norbornanone
1,3,3Trimethyl2norcamphanone
2Norbornanone, 1,3,3trimethyl
1,3,3Trimethylbicyclo(2.2.1)heptan2one
CAS-1195-79-5
Bicyclo(2.2.1)heptan2one, 1,3,3trimethyl
Bicyclo2.2.1heptan-2-one, 1,3,3-trimethyl-, (1S,4R)-
214-804-6
fenchone, (+-)-isomer
2-Norbornanone, 1,3,3-trimethyl-
126-21-6
D-FENCHONE, 96
NCGC00166292-01
1,3-Trimethylnorcamphor
1,3-Trimethyl-2-norbornanone
1,3-Trimethyl-2-norcamphanone
2-Norbornanone,3,3-trimethyl-
WLN: L55 A CVTJ B1 D1 D1
1,3-Trimethylbicyclo[2.2.1]heptan-2-one
Bicyclo[2.2.1]heptan-2-one,3,3-trimethyl-
iso-Fenchone
MFCD00151104
(1R)-1,3,3-Trimethylbicyclo[2.2.1]heptan-2-one
SCHEMBL57584
CHEMBL2268554
NSC8896
Tox21_112396
BBL018824
MFCD00248429
NSC122687
s5934
STK802502
AKOS009158536
LMPR0102120016
VS-06784
DB-017638
DB-070766
F0163
F0164
NS00012481
1.3.3-trimethylbicyclo(2.2.1)heptan-2-one
EN300-54085
C09859
SBI-0653876.0001
1,3,3-Trimethyl-bicyclo[2.2.1]heptan-2-one
Bicyclo[2.2.1]heptane-2-one,1,3,3-trimethyl
Q414784
SR-01000945193
SR-01000945193-1
Z804948554
Bicyclo[2.2.1]heptan-2-one, 1,3,3-trimethyl-, (.+/-.)-
Solubility of 1,3,3-trimethylnorbornan-2-one
1,3,3-trimethylnorbornan-2-one, a polycyclic ketone, exhibits some interesting characteristics regarding its solubility. When considering the solubility of this compound, it's important to recognize the following aspects:
In summary, the solubility of 1,3,3-trimethylnorbornan-2-one is largely dictated by its hydrocarbon structure and overall polarity. This compound is generally soluble in non-polar solvents, making it important for applications where such compatibility is essential.