Interesting facts
Interesting Facts about (1R,2R)-1,2-Dimethylcyclohexane
(1R,2R)-1,2-Dimethylcyclohexane is an intriguing organic compound known for its unique structure and stereochemistry. Here are some fascinating aspects of this compound:
- Stereochemistry: The designation (1R,2R) refers to the specific configuration of the chiral centers in the cyclohexane ring. This stereochemistry is crucial because it influences the compound's reactivity and properties.
- Lock and Key Model: The spatial arrangement of the methyl groups affects how the compound interacts with other molecules. It exemplifies the lock and key model in organic chemistry, where the shape of the molecule determines its biochemical interactions.
- Cyclohexane Chair Conformation: This compound can exist in multiple conformations, but the chair conformation is the most stable. In this form, the methyl groups can occupy axial or equatorial positions, further influencing the compound's stability and reactivity.
- Industry Relevance: Dimethylcyclohexanes are often used as solvents and in the production of various chemical substances, making them valuable in industrial applications.
- Rotational Freedom: The cyclohexane ring provides a degree of rotational freedom, which allows chemists to study the effects of conformational changes on molecular properties, leading to a deeper understanding of sterics and electronic interactions.
These features not only make (1R,2R)-1,2-dimethylcyclohexane a subject of study in academic research but also highlight its significance in practical applications, shedding light on the intricate relationship between molecular structure and function.
Synonyms
trans-1,2-Dimethylcyclohexane
6876-23-9
1,trans-2-Dimethylcyclohexane
HKG4AHC8VR
1,2-Dimethylcyclohexane, trans-
NSC 74158
1,2-trans-Dimethylcyclohexane
Cyclohexane, 1,2-dimethyl-, (1R,2R)-rel-
EINECS 229-979-4
AI3-28850
DTXSID30858753
NSC-74158
CYCLOHEXANE, 1,2-DIMETHYL-, (E)
DTXCID50809484
Cyclohexane, 1,2-dimethyl-, trans-(8CI)
(+-)-TRANS-1,2-DIMETHYLCYCLOHEXANE
Cyclohexane, 1,2-dimethyl-, trans-(8CI)(9CI)
229-979-4
(1R,2R)-1,2-dimethylcyclohexane
trans-Hexahydro-o-xylene
SJL41NX55V
Cyclohexane, 1,2-dimethyl-, trans-
UNII-SJL41NX55V
1,2-Dimethylcyclohexane, (1R,2R)-
Cyclohexane, 1,2-dimethyl-, (1R,2R)-
203319-65-7
1,2-dimethyl(trans)-cyclohexane
UNII-HKG4AHC8VR
t-1,2-Dimethylcyclohexane
trans-1,2-dimethyl-cyclohexane
CHEBI:188237
Cyclohexane, trans-1,2-dimethyl-
LMFA11000637
trans-1,2-Dimethylcyclohexane, 99%
(1R)-trans-1,2-dimethyl-cyclohexane
AKOS015913284
D0697
(+/-)-TRANS-1,2-DIMETHYLCYCLOHEXANE
Solubility of (1R,2R)-1,2-dimethylcyclohexane
(1R,2R)-1,2-dimethylcyclohexane, a bicyclic organic compound, exhibits some interesting characteristics regarding its solubility. Here are some key points to consider:
In summary, the solubility of (1R,2R)-1,2-dimethylcyclohexane showcases the principles of solubility in action, emphasizing the significance of molecular structure in determining the compatibility with solvents. As stated, "like dissolves like," and this compound serves as a prime example of that concept.