Interesting facts
Interesting Facts About 1,7,7-Trimethylnorbornane-2,3-dione
1,7,7-trimethylnorbornane-2,3-dione is a fascinating compound that offers a wealth of intriguing characteristics for chemists and researchers alike. Here are some notable aspects:
- Unique Structural Features: This compound belongs to the class of norbornene derivatives, known for their intriguing bicyclic structure. The presence of multiple methyl groups on the norbornane backbone creates steric hindrance that can influence its reactivity and stability.
- Versatile Applications: Due to its diketone nature, this compound acts as a crucial intermediate in organic synthesis. It can be utilized in the formation of various derivatives, which broadens its applicability in fields such as pharmaceuticals and materials science.
- Reactivity Insights: The two carbonyl (C=O) groups make 1,7,7-trimethylnorbornane-2,3-dione a potential candidate for nucleophilic addition reactions. This reactivity opens doors for further transformations, allowing chemists to innovate and design new compounds.
- Significance in Stereochemistry: The symmetrical nature of this compound introduces an interesting perspective for studying stereochemical outcomes, particularly in terms of how different substituents may affect molecular interactions and equilibria.
- Analytical Interest: Its unique structure and reactivity make it an interesting target for spectroscopic methods, including NMR and IR spectroscopy, allowing students and scientists to refine their analytical skills.
In summary, 1,7,7-trimethylnorbornane-2,3-dione stands out not only for its structural properties but also for its potential applications and implications in various scientific fields. As you explore this compound, consider how its distinct characteristics can lead to new discoveries in synthesis and reactivity!
Synonyms
Camphorquinone
2,3-Bornanedione
1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione
bornane-2,3-dione
Camphor quinone
Camphoquinone
CHEBI:34607
1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione bornane-2,3-dione
1,7,7-TRIMETHYLBICYCLO(2.2.1)HEPTANE-2,3-DIONE
1,7,7-trimethylbicyclo(2.2.1)heptane-2,3-dione bornane-2,3-dione
207-363-6
10373-78-1
DL-CAMPHORQUINONE
Camphoroquinone
465-29-2
(+/-)-Camphorquinone
DTXSID7049394
( inverted exclamation markA)-Camphorquinone
Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1R)-
CAMPHOREQUINONE
Bicyclo[2.2.1]heptane-2, 1,7,7-trimethyl-
1,7,7-trimethylbicyclo(2.2.1)heptan-2,3-dione
(1R)-(-)-2,3-Bornanedione
3-Ketocamphor
dl-Camphoroquinone
1,7,7-trimethylnorbornane-2,3-dione
(+/-) camphorquinone
(1R)-(-)-Camphorquinon
SCHEMBL15201
CHEMBL301431
NSC285
DTXCID4029353
(1S)-(+)-2,3-Bornanedione
Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1S)-
Tox21_202961
BBL012870
NSC402031
STK803340
AKOS001042401
AKOS016037995
FC40615
LMPR0102120030
NCGC00260507-01
AS-15119
SY036381
CAS-10373-78-1
DB-047258
DB-058983
DB-059044
DB-286103
C1660
CS-0127185
NS00019583
NS00080204
ST50307377
EN300-17476
N11921
1,7,7-trimethyl-bicyclo[2.2.1]heptane-2,3-dione
Q2698440
1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-dione #
Z56943556
2,3-Bornanedione;1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
Solubility of 1,7,7-trimethylnorbornane-2,3-dione
The solubility of 1,7,7-trimethylnorbornane-2,3-dione (C10H14O2) can be quite intriguing due to its unique structural characteristics. Understanding its solubility involves a few key considerations:
In summary, while exact solubility data may be limited, one can anticipate that 1,7,7-trimethylnorbornane-2,3-dione would demonstrate better solubility in polar solvents compared to its non-polar counterparts. Its unique characteristics suggest interesting behavior that may warrant further investigation.