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Ethyl cyclohexanecarboxylate

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Identification
Molecular formula
C9H16O2
CAS number
1671-91-6
IUPAC name
ethyl cyclohexanecarboxylate
State
State

At room temperature, ethyl cyclohexanecarboxylate is a liquid. It is non-crystalline and has a relatively low viscosity.

Melting point (Celsius)
-67.00
Melting point (Kelvin)
206.15
Boiling point (Celsius)
214.00
Boiling point (Kelvin)
487.15
General information
Molecular weight
156.22g/mol
Molar mass
156.2220g/mol
Density
0.9519g/cm3
Appearence

Ethyl cyclohexanecarboxylate is a colorless liquid with a pleasant, fruity odor. It is often used in the fragrance and flavor industries due to its aromatic properties.

Comment on solubility

Solubility of Ethyl Cyclohexanecarboxylate

Ethyl cyclohexanecarboxylate is an interesting compound when it comes to its solubility properties. This alkyl ester tends to exhibit the following characteristics:

  • Nonpolar Nature: Due to the cyclohexane ring, ethyl cyclohexanecarboxylate displays a nonpolar character, typically limiting its ability to dissolve in highly polar solvents like water.
  • Solvents: It is more soluble in organic solvents such as:
    • Hexane
    • Ether
    • Alcohols
  • Temperature Dependency: The solubility of ethyl cyclohexanecarboxylate can also be affected by temperature, often increasing with rising temperatures in organic solvents.
  • Practical Applications: This solubility behavior makes ethyl cyclohexanecarboxylate suitable for applications in organic synthesis and as a solvent for various reactions involving nonpolar materials.

In summary, while ethyl cyclohexanecarboxylate is not soluble in water, its compatibility with nonpolar and slightly polar solvents makes it a versatile compound in the realm of organic chemistry.

Interesting facts

Interesting Facts about Ethyl Cyclohexanecarboxylate

Ethyl cyclohexanecarboxylate is an intriguing compound that belongs to the family of carboxylic esters. Its unique structure and properties offer a variety of applications and potential in the realm of organic chemistry. Here are some notable aspects:

  • Versatile Building Block: Ethyl cyclohexanecarboxylate serves as a vital building block in organic synthesis. It is often used in the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals.
  • Esters in Action: Like many esters, this compound exhibits pleasant and fruity odors, making it an interesting candidate for flavor and fragrance applications.
  • Reaction Enthusiast: Ethyl cyclohexanecarboxylate is prone to undergo nucleophilic acyl substitution reactions, making it a useful reagent in organic reactions aimed at producing more complex molecules.
  • Environmental Considerations: The compound's derivation from renewable resources has garnered attention due to the growing emphasis on sustainability in chemical production.
  • Research Applications: It is sometimes utilized in various research studies to explore its reactivity and interaction with different functional groups, helping to uncover new pathways in synthetic chemistry.

The rich chemistry surrounding ethyl cyclohexanecarboxylate highlights its importance in both industrial applications and academic research. As stated by chemists, this compound exemplifies the beauty in the complexity of organic synthesis, reinforcing the notion that "every molecule tells a story."

Synonyms
Ethyl cyclohexanecarboxylate
cyclohexanecarboxylic acid ethyl ester
Ethyl hexahydrobenzoate
CYCLOHEXANECARBOXYLIC ACID, ETHYL ESTER
Ethoxycarbonylcyclohexane
ethyl cyclohexanoate
Ethyl cyclohexylcarboxylate
FEMA No. 3544
EINECS 221-945-7
BRN 2042698
UNII-87937T10YQ
AI3-07031
NSC-5298
87937T10YQ
DTXSID7062958
CHEBI:88965
FEMA 3544
4-09-00-00018 (Beilstein Handbook Reference)
ETHYL CYCLOHEXANECARBOXYLATE [FHFI]
DTXCID7038600
221-945-7
jjoychkvkwdmea-uhfffaoysa-n
3289-28-9
Ethyl cyclohexylformate
Ethyl cyclohexylmethanoate
Ethyl cylcohexanecarboxylate
NSC 5298
MFCD00041734
Ethyl cyclohexanocarboxylate
ethyl cyclohexane carboxylate
Ethylcyclohexanecarboxylate
2-ethoxycarbonylcyclohexane
4-ethoxycarbonylcyclohexane
ethyl cyclohexyl-carboxylate
SCHEMBL18888
ethyl 2-cyclohexanecarboxylate
ethyl 4-cyclohexanecarboxylate
NSC5298
DAA28928
AKOS005255069
cyclohexane carboxylic acid ethyl ester
AS-15352
DB-013160
CS-0187422
NS00022058
E77025
EN300-155929
Q27161060
Z53835749