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3-cyclopent-2-en-1-yloxycyclopentene

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Identification
Molecular formula
C10H14O
CAS number
40504-37-2
IUPAC name
3-cyclopent-2-en-1-yloxycyclopentene
State
State

At room temperature, it is in a liquid state.

Melting point (Celsius)
-48.00
Melting point (Kelvin)
225.15
Boiling point (Celsius)
210.00
Boiling point (Kelvin)
483.15
General information
Molecular weight
148.21g/mol
Molar mass
148.2060g/mol
Density
0.9500g/cm3
Appearence

The compound is typically a colorless liquid. It may exhibit a slight yellow hue depending on the purity and the presence of any impurities.

Comment on solubility

Solubility of 3-cyclopent-2-en-1-yloxycyclopentene

The solubility of 3-cyclopent-2-en-1-yloxycyclopentene in various solvents can be intriguing given its unique structure. This compound, being an organic molecule, exhibits solubility characteristics influenced by several factors:

  • Polar vs Nonpolar Solvents: Generally, organic compounds like this one tend to be more soluble in nonpolar solvents such as hexane or benzene, rather than in polar solvents like water.
  • Functional Groups: The presence of ether functional groups may contribute to solubility in some polar organic solvents, though steric hindrance from the cyclopentene rings could limit this effect.
  • Molecular Size: The relatively moderate molecular size may assist in solubilizing in certain organic solvents while presenting challenges in highly polar environments.

It is often said, “Like dissolves like,” and in the case of 3-cyclopent-2-en-1-yloxycyclopentene, this adage holds, guiding the selection of appropriate solvents for dissolution experiments. The exploration of its solubility can provide further insight into its potential applications and behaviors in chemical processes.

Interesting facts

Exploring 3-Cyclopent-2-en-1-yloxycyclopentene

3-Cyclopent-2-en-1-yloxycyclopentene, a compound with intriguing structural characteristics, belongs to the class of organic compounds known as cyclic ethers. Here are some fascinating points about this remarkable compound:

  • Unique Structure: The compound features a bicyclic framework that combines two cyclopentene rings. This structural arrangement contributes to its potential reactivity and stability.
  • Chemical Reactivity: The presence of both the enolic double bond and the ether functional group makes it a potential subject of study for reactions such as Diels-Alder cycloadditions, which are pivotal in organic synthesis.
  • Applications in Material Science: Compounds like 3-cyclopent-2-en-1-yloxycyclopentene can serve as intermediates in the synthesis of advanced materials, particularly in the production of polymers and specialized coatings.
  • Potential in Pharmaceuticals: The unique features of cyclic compounds often contribute to their biological activity. Research into such structures may yield new pharmaceuticals with novel mechanisms of action.

As a compound that exemplifies the complexity and diversity of organic molecules, 3-Cyclopent-2-en-1-yloxycyclopentene highlights the importance of understanding its properties and potential uses in various fields of chemistry. As the saying goes, "In chemistry, complexity leads to opportunities!"

This compound represents just one of the many exciting avenues for exploration in organic chemistry, inviting researchers and students alike to delve deeper into its potential applications and properties.

Synonyms
Cyclopentene, 3,3'-oxybis-
Bis(cyclopent-2-enyl) ether
Diene 205
ETHER, BIS(2-CYCLOPENTENYL)
Cyclopentene, 3,3-prime-oxybis-
NSC 2486
EINECS 239-195-4
BRN 1943489
DTXSID80884789
3-06-00-00203 (Beilstein Handbook Reference)
DTXCID301024212
Cyclopentene, 3,3'-oxybis-(9CI)
239-195-4
2-Cyclopenten-1-yl ether
15131-55-2
3-cyclopent-2-en-1-yloxycyclopentene
2-CYCLOPENTEN-1-YL ETHER, 98
Cyclopentene,3'-oxybis-
WLN: L5UTJ CO- CL5UTJ
NSC2486
SCHEMBL538101
NSC4163
NSC-2486
NSC-4163
AKOS006230271
NS00051416
3-(2-Cyclopenten-1-yloxy)-1-cyclopentene #