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Ethyl norbornene-2-carboxylate

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Identification
Molecular formula
C10H14O2
CAS number
1641-17-4
IUPAC name
ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate
State
State

At room temperature, ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate is a liquid.

Melting point (Celsius)
-37.50
Melting point (Kelvin)
235.70
Boiling point (Celsius)
202.70
Boiling point (Kelvin)
475.90
General information
Molecular weight
166.22g/mol
Molar mass
166.2230g/mol
Density
0.9757g/cm3
Appearence

Ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate appears as a colorless liquid. It is often used as an intermediate in organic syntheses.

Comment on solubility

Solubility of Ethyl Bicyclo[2.2.1]hept-5-ene-2-carboxylate (C10H14O2)

Ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate exhibits interesting solubility characteristics that depend on several factors:

  • Polarity: As a compound with both aliphatic (bicyclic) and carboxylate elements, its polarity influences solubility in various solvents.
  • Nonpolar Solvents: It shows better solubility in nonpolar solvents such as hexane or toluene due to its hydrocarbon structure, which minimizes interactions with polar components.
  • Polar Solvents: Conversely, its limited polar characteristics result in reduced solubility in water and other polar solvents.
  • Temperature: Increased temperatures can enhance solubility for many organic compounds, suggesting that heating may improve its dissociation in specific solvents.

In summary, while ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate can be soluble in nonpolar environments, its interaction with polar solvents remains minimal. As noted, understanding solubility is crucial for applications ranging from synthetic reactions to pharmaceuticals, embodying the statement: "Solubility is a key to chemical behavior."

Interesting facts

Interesting Facts about Ethyl Bicyclo[2.2.1]hept-5-ene-2-carboxylate

Ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate is a unique compound characterized by its interesting bicyclic structure, which offers a diverse range of chemical properties and applications. Here are some compelling insights into this compound:

  • Bicyclic Charm: The bicyclic framework of this compound adds to its stability and reactivity, making it a subject of interest for synthetic chemists looking to create complex molecules.
  • Versatile Reactivity: Due to its structural features, this compound can participate in various chemical reactions, including Diels-Alder reactions and nucleophilic additions, which are valuable in organic synthesis.
  • Natural Product Precursor: This compound can be considered as a precursor to various natural products and pharmaceuticals, highlighting its importance in medicinal chemistry.
  • Odor and Flavor Research: Compounds with similar structures often exhibit distinct aromas and flavors, making this compound a potential candidate for research in the fragrance and food industries.

As noted by many researchers, "understanding the reactivity of bicyclic compounds opens new avenues for synthesis and innovation." Thus, the study of ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate not only enhances our understanding of organic chemistry but also paves the way for developing new materials and medicines.

In conclusion, the intricate structure and reactivity of ethyl bicyclo[2.2.1]hept-5-ene-2-carboxylate render it a fascinating compound worth exploring for any chemistry enthusiast or professional!

Synonyms
10138-32-6
ETHYL BICYCLO[2.2.1]HEPT-5-ENE-2-CARBOXYLATE
Bicyclo[2.2.1]hept-5-ene-2-carboxylic acid, ethyl ester
Ethyl 5-norbornene-2-carboxylate
NSC 26489
QEA96R4A1Z
BICYCLO(2.2.1)HEPT-5-ENE-2-CARBOXYLIC ACID, ETHYL ESTER
DTXSID30884451
NSC-26489
NSC-62714
ETHYL BICYCLO(2.2.1)HEPT-5-ENE-2-CARBOXYLATE
5-ethoxycarbonylnorbornene
FEMA NO. 4790
DTXCID701023892
5-NORBORNENECARBOXYLIC ACID ETHYL ESTER
5-Norbornene-2-carboxylic acid, ethyl ester
WLN: L55 A CUTJ FVO2
ethyl bicyclo[2.2.1]hept-2-ene-5-carboxylate
UNII-QEA96R4A1Z
NSC26489
2,5-Endomethylene-3-cyclohexene carboxylic acid, ethyl ester
NCIOpen2_000131
2-ethoxycarbonyl-5-norbornene
SCHEMBL200507
SCHEMBL2774448
SCHEMBL7524542
FCCGTJAGEHZPBF-UHFFFAOYSA-N
NSC62714
SBB060557
AKOS015917768
AC-4862
AS-75467
DB-058601
ST50443849
E77868