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Cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate

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Identification
Molecular formula
C14H20O2
CAS number
.569539-95-5
IUPAC name
cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate
State
State

At room temperature, this compound exists as a liquid. It is less dense than water, with a tendency to form a separate phase when mixed with aqueous solutions.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
220.32g/mol
Molar mass
220.3170g/mol
Density
1.0000g/cm3
Appearence

This compound typically appears as a colorless to pale yellow liquid. The appearance can vary depending on purity and specific conditions under which it is observed.

Comment on solubility

Solubility of Cyclohex-3-en-1-ylmethyl Cyclohex-3-ene-1-carboxylate

The solubility of cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate can be quite intriguing due to its unique structure. Several factors influence its solubility, including:

  • Polarity: The presence of the carboxylate group contributes to a degree of polarity, which can facilitate interactions with polar solvents such as water.
  • Size and Shape: The cyclohexene rings and bulky groups may hinder its ability to dissolve in certain solvents, affecting overall solubility.
  • Temperature: Like many organic compounds, solubility can increase with temperature, enhancing the likelihood of dissolution in appropriate solvents.

It is essential to consider the following points:

  • The compound is likely to be more soluble in organic solvents (e.g., ethanol, acetone) than in water due to the hydrophobic nature of the cyclohexene rings.
  • Integrating various solvents may lead to better solubilization, as “like dissolves like” principle applies here.

In summary, while cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate exhibits limited solubility in water, it can be effectively dissolved in a range of organic solvents. Therefore, understanding its solubility profile is crucial for its applications and handling in laboratory settings.

Interesting facts

Interesting Facts about Cyclohex-3-en-1-ylmethyl Cyclohex-3-ene-1-carboxylate

Cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate is a fascinating compound that showcases the complexities of organic chemistry. Here are some key points that highlight its significance:

  • Structural Diversity: This compound features two cyclohexene rings, which provide a unique arrangement that can influence its chemical properties and reactivity. The ability to manipulate such structures opens up various pathways for synthetic chemistry.
  • Application in Synthesis: Cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate serves as an important building block in organic synthesis, particularly in the creation of more complex molecules. Its versatile structure allows chemists to explore new synthetic routes.
  • Potential in Drug Development: Compounds similar to cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate have shown promise in medicinal chemistry. Their unique properties may contribute to the development of pharmaceutical agents with enhanced efficacy.
  • Reactivity: The presence of the enone functional group allows for interesting reactivity, including the potential for Diels-Alder reactions, which is a valuable tool in creating cyclic compounds with high stereocontrol.
  • Research Interest: As a subject of ongoing research, this compound can be used to study reaction mechanisms and dynamics, providing insights into fundamental principles of organic chemistry.

In summary, cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate exemplifies the intricate world of organic compounds. As one delves deeper into its structure and applications, one may discover the vast potential that such compounds hold for future explorations in chemistry.

Synonyms
2611-00-9
3-Cyclohexene-1-carboxylic acid, 3-cyclohexen-1-ylmethyl ester
Diene 221
3-Cyclohexenyl 3-cyclohexene 1-carboxylate
3-CYCLOHEXENYLMETHYL 3-CYCLOHEXENECARBOXYLATE
HSDB 5887
E31OX8KGAL
EINECS 220-031-5
NSC 49615
Cyclohex-3-enylmethyl cyclohex-3-enecarboxylate
NSC-49615
DTXSID9027493
3-CYCLOHEXENE-1-CARBOXYLIC ACID 3-CYCLOHEXENYLMETHYL ESTER
3-CYCLOHEXEN-1-YLMETHYL 3-CYCLOHEXENECARBOXYLATE
3-CYCLOHEXENYL 3-CYCLOHEXENE 1-CARBOXYLATE [HSDB]
3-CYCLOHEXENYLMETHYL 3'-CYCLOHEXENE-1-CARBOXYLATE
1,2,5,6-TETRAHYDROBENZYL 1,2,5,6-TETRAHYDROBENZOATE
DTXCID407493
Cyclohex3enylmethyl cyclohex3enecarboxylate
3Cyclohexene1carboxylic acid, 3cyclohexen1ylmethyl ester
220-031-5
Cyclohex-3-en-1-ylmethyl cyclohex-3-enecarboxylate
cyclohex-3-en-1-ylmethyl cyclohex-3-ene-1-carboxylate
UNII-E31OX8KGAL
NSC49615
MFCD00169071
1-cyclohex-3-enylmethyl cyclohex-3-ene-1-carboxylate
SCHEMBL472104
FJPFRSQDAFMEKD-UHFFFAOYSA-N
WLN: L6UTJ DVO1- CL6UTJ
AKOS015915506
BS-52128
CS-0199063
NS00021955
Cyclohex-3-en-1-ylmethylcyclohex-3-enecarboxylate
Q27276802