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1-Ethoxynaphthalene

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Identification
Molecular formula
C12H12O
CAS number
1126-34-7
IUPAC name
1-ethoxynaphthalene
State
State

At room temperature, 1-ethoxynaphthalene is a liquid. It remains stable under normal conditions of use and storage, demonstrating typical properties expected of an ether.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
263.00
Boiling point (Kelvin)
536.15
General information
Molecular weight
172.22g/mol
Molar mass
172.2220g/mol
Density
1.0610g/cm3
Appearence

1-Ethoxynaphthalene appears as a colorless to pale yellow liquid. Its clarity can make it challenging to observe in certain containers, but its distinct aromatic odor is often a giveaway of its presence.

Comment on solubility

Solubility of 1-Ethoxynaphthalene

1-Ethoxynaphthalene, with the chemical formula C12H12O, exhibits interesting solubility characteristics which can be summarized as follows:

  • Solvent Characteristics: 1-Ethoxynaphthalene is generally soluble in non-polar and organic solvents such as:
    • Benzene
    • Toluene
    • Chloroform
  • Limited Water Solubility: This compound is known to be practically insoluble in water, which is a common trait for many organic compounds due to their hydrophobic nature.
  • Temperature Effects: The solubility of 1-ethoxynaphthalene can vary with temperature, often increasing as the temperature rises, making it more favorable in warmer conditions.

As with many organic compounds, solubility factors such as molecular structure, polarity, and the type of solvent play crucial roles in determining the extent of solubility. Consequently, 1-ethoxynaphthalene serves as a valuable compound in organic synthesis and various industrial applications, thanks to its solubility profile.

Interesting facts

Interesting Facts About 1-Ethoxynaphthalene

1-Ethoxynaphthalene is a fascinating organic compound belonging to the naphthalene family, and it exhibits unique properties and applications that intrigue chemists and chemical engineers alike. Here are some notable aspects of this compound:

  • Structural Characteristics: 1-Ethoxynaphthalene consists of a naphthalene nucleus substituted with an ethoxy group. This ethoxy substitution significantly alters the compound's properties compared to unsubstituted naphthalene, demonstrating how minor structural changes can lead to diverse chemical behaviors.
  • Applications: This compound finds its use in various fields, including:
    • As a solvent or reagent in organic synthesis.
    • In the preparation of specialty chemicals such as fragrances and dyes.
    • In studying the electronic and spectroscopic properties of aromatic compounds.
  • Scientific Importance: 1-Ethoxynaphthalene serves as a model compound in the study of:
    • Substituent effects on reactivity and stability.
    • Fluorescence properties and interactions with other molecules.
  • Chemical Behavior: The presence of the ethoxy group affects the compound’s reactivity, making it less electrophilic compared to naphthalene. This distinction provides an opportunity to explore substitution reactions in a controlled manner.
  • Research Opportunities: With ongoing advancements in organic chemistry, 1-ethoxynaphthalene may pave the way for the development of new materials and the fine-tuning of chemical processes.

In summary, 1-ethoxynaphthalene is more than just a simple derivative of naphthalene; it represents a rich area of study that can lead to insights in reactivity, synthesis, and applications in various scientific fields. Its modification and behavior exemplify the beauty of organic chemistry, where slight changes can lead to monumental discoveries.

Synonyms
1-ETHOXYNAPHTHALENE
Ethyl 1-naphthyl ether
KPT9T4S9QZ
NSC-4174
DTXSID30201402
NSC 4174
EINECS 226-213-0
AI3-00179
DTXCID90123893
apwzaiznwqfzbk-uhfffaoysa-n
5328-01-8
Naphthalene, 1-ethoxy-
1-Ehoxynaphthalene
.alpha.-Ethoxynaphthalene
alpha-Ethoxynaphthalene
Ethyl alpha-naphthyl ether
Ethyl .alpha.-naphthyl ether
Naphthalene, ethoxy-
ethoxynaphthalene
MFCD00003928
UNII-KPT9T4S9QZ
1-ETHOXY-NAPHTHALIN
SCHEMBL45343
NSC4174
CHEBI:167813
GEO-01305
AKOS002945485
LS-14062
DB-019161
CS-0197266
E0532
NS00015729
EN300-52462
D90537
Z55021536