Interesting facts
Interesting Facts about 1-Ethyl-4-methyl-cyclohexane
1-Ethyl-4-methyl-cyclohexane is a fascinating compound in organic chemistry with several intriguing aspects:
- Structure: As a derivative of cyclohexane, this compound features a unique ring structure with both ethyl and methyl substituents. This arrangement contributes to its distinctive chemical properties.
- Synthesis: The synthesis of 1-Ethyl-4-methyl-cyclohexane can involve various methods, including alkylation reactions. Such reactions showcase the versatility of organic synthesis techniques.
- Isomerism: This compound is just one of many isomers of C10H18. Understanding its isomeric forms can enhance our comprehension of its reactivity and stability.
- Applications: While 1-Ethyl-4-methyl-cyclohexane may not have widespread industrial applications, compounds with similar structures often play essential roles in the production of pharmaceuticals, agrochemicals, and even fragrance chemistry.
- Research Potential: Its relatively simple structure makes it a great candidate for studies related to conformational analysis and stereochemistry. Researchers often explore how even small changes in structure can significantly affect reactivity.
- Safety and Handling: Like many organic compounds, handling 1-Ethyl-4-methyl-cyclohexane requires safety measures due to its flammability and potential health effects. Proper precautions should always be observed in the laboratory.
In summary, 1-Ethyl-4-methyl-cyclohexane serves not only as a model compound for theoretical studies but also illuminates many important concepts in organic chemistry. It’s a prime example of how a simple structure can lead to complex chemical behavior.
Synonyms
1-Ethyl-4-methylcyclohexane
DTXSID00190733
DTXCID40113224
3728-56-1
cis-1-Ethyl-4-Methylcyclohexane
trans-1-Ethyl-4-Methylcyclohexane
4926-78-7
6236-88-0
Cyclohexane, 1-ethyl-4-methyl-, cis-
Cyclohexane, 1-ethyl-4-methyl-, trans-
cis-1-ethyl-4-methycyclohexane
trans-1-ethyl-4-methycyclohexane
Cyclohexane, 1-ethyl-4-methyl-
1-Ethyl-4-methylcyclohexane cis-
Cis-1-ethyl-4-methyl cyclohexane
1-Ethyl-4-methylcyclohexane trans-
1-ethyl-4-methyl(trans)-cyclohexane
MFCD00045511
1-ethyl-4-methyl-cyclohexane
c-1-Ethyl-4-methylcyclohexane
1-Methyl-cis-4-ethylcyclohexane
cis-1-Methyl-4-Ethylcyclohexane
CYISMTMRBPPERU-DTORHVGOSA-N
CYISMTMRBPPERU-KYZUINATSA-N
1-Methyl-trans-4-ethylcyclohexane
DTXSID001025635
DTXSID201015854
trans-1-Methyl-4-Ethylcyclohexane
1-ethyl-4-methyl(cis)-cyclohexane
1-Ethyl-4-methylcyclohexane, (E)-
1-Ethyl-4-methylcyclohexane, (Z)-
1-Ethyl-4-methylcyclohexane, trans-
LMFA11000649
LMFA11000650
AKOS006274115
AKOS006274116
DB-049090
DB-318923
CS-0451769
E0424
T72381
Solubility of 1-ethyl-4-methyl-cyclohexane
1-ethyl-4-methyl-cyclohexane is an organic compound that exhibits distinct solubility characteristics due to its molecular structure. Key points about its solubility include:
In summary, the solubility of 1-ethyl-4-methyl-cyclohexane can be summarized by the phrase: "Like dissolves like." Therefore, it is best suited for nonpolar environments rather than polar solvents such as water.