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1-ethyl-2-methylcyclopentane

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Identification
Molecular formula
C8H16
CAS number
15625-35-9
IUPAC name
(1R,2R)-1-ethyl-2-methyl-cyclopentane
State
State

At room temperature, 1-ethyl-2-methylcyclopentane is in a liquid state.

Melting point (Celsius)
-123.00
Melting point (Kelvin)
150.15
Boiling point (Celsius)
113.40
Boiling point (Kelvin)
386.55
General information
Molecular weight
98.19g/mol
Molar mass
98.1870g/mol
Density
0.7496g/cm3
Appearence

1-ethyl-2-methylcyclopentane typically appears as a colorless liquid under standard conditions. It is a hydrocarbon, which means it consists solely of carbon and hydrogen atoms.

Comment on solubility

Solubility of (1R,2R)-1-ethyl-2-methyl-cyclopentane

The solubility of (1R,2R)-1-ethyl-2-methyl-cyclopentane, a cyclic hydrocarbon, is primarily influenced by its hydrophobic nature. Being a non-polar compound, it tends to be insoluble in polar solvents such as water.

Here are some essential points regarding its solubility:

  • Non-polar characteristics: The symmetrical structure of the cyclopentane ring, combined with the ethyl and methyl substituents, creates a non-polar molecule.
  • Insolubility in water: Due to the absence of polar functional groups, (1R,2R)-1-ethyl-2-methyl-cyclopentane does not dissolve in water.
  • Soluable in organic solvents: It shows good solubility in non-polar organic solvents, such as hexane and benzene.

In summary, despite its structural complexity, the solubility of (1R,2R)-1-ethyl-2-methyl-cyclopentane can be succinctly characterized: insoluble in water and highly soluble in non-polar organic solvents. This distinction is significant for understanding its behavior in various chemical environments.

Interesting facts

Interesting Facts about (1R,2R)-1-ethyl-2-methyl-cyclopentane

(1R,2R)-1-ethyl-2-methyl-cyclopentane is a fascinating organic compound that belongs to the category of cyclic hydrocarbons known as cyclopentanes. Here are some remarkable aspects of this compound:

  • Chirality and Isomerism: The (1R,2R) notation indicates that this compound has a specific chiral configuration. Chirality is crucial in many fields, especially in pharmaceuticals, where the activity of a compound can vary dramatically between enantiomers.
  • Structural Diversity: With its unique arrangement of ethyl and methyl groups on the cyclopentane ring, this compound showcases structural diversity that can lead to different physical and chemical properties, influencing how it interacts with other molecules.
  • Applications in Organic Synthesis: Compounds like (1R,2R)-1-ethyl-2-methyl-cyclopentane serve as intermediates in organic synthesis. They can be transformed into more complex structures necessary for drug development and other applications.
  • Research Interests: Scientists are keenly interested in the study of cycloalkanes, including (1R,2R)-1-ethyl-2-methyl-cyclopentane, for developing new materials, optimizing reaction mechanisms, and exploring novel catalytic processes.

In summary, (1R,2R)-1-ethyl-2-methyl-cyclopentane is more than just a simple organic compound; it represents the intricate world of chemistry where structural configuration plays a critical role in determining the behavior and functionality of molecules. As highlighted by chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas,” which rings true in the exploration of such compounds!

Synonyms
trans-1-Ethyl-2-methylcyclopentane
EINECS 213-227-7
Cyclopentane, 1-ethyl-2-methyl-, (1R,2R)-rel-
rel-(1R,2R)-1-Ethyl-2-methylcyclopentane
213-227-7
930-90-5
DTXSID2075055
BSKOLJVTLRLTHE-HTQZYQBOSA-N
trans-1-Methyl-2-ethylcyclopentane
1-Ethyl-2-methylcyclopentane, trans
trans-1-Ethyl-2-methyl-cyclopentane
1-ethyl-2-methyl(trans)-cyclopentane
rac-(1R,2R)-1-ethyl-2-methylcyclopentane
NS00039523
EN300-22044075