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6-Ethyltetralin

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Identification
Molecular formula
C12H16
CAS number
1573-59-1
IUPAC name
6-ethyltetralin
State
State

At room temperature, 6-Ethyltetralin is in a liquid state, typical for many hydrocarbons of similar molecular weight.

Melting point (Celsius)
-48.00
Melting point (Kelvin)
225.15
Boiling point (Celsius)
227.00
Boiling point (Kelvin)
500.15
General information
Molecular weight
160.27g/mol
Molar mass
160.2680g/mol
Density
0.9058g/cm3
Appearence

6-Ethyltetralin appears as a colorless liquid under standard conditions.

Comment on solubility

Solubility of 6-ethyltetralin

6-ethyltetralin, a compound characterized by its unique molecular structure, exhibits interesting solubility properties:

  • Solubility in Organic Solvents: 6-ethyltetralin is significantly soluble in various organic solvents such as benzene, toluene, and ether. This solubility is largely attributed to its hydrophobic characteristics.
  • Poor Water Solubility: In contrast, 6-ethyltetralin shows minimal solubility in water, which is common among non-polar organic compounds. This limited solubility in polar solvents often influences its practical applications.
  • Temperature Effects: The solubility can vary with temperature; increased temperatures typically lead to higher solubility in organic solvents.
  • Impurities Impact: The presence of impurities or other solutes may significantly alter the solubility profile of 6-ethyltetralin, highlighting the importance of purity in solubility studies.

In summary, when considering the solubility of 6-ethyltetralin, take note of its affinity for organic environments and the challenges it poses in aqueous solutions. As with many hydrophobic compounds, understanding its solubility can be key to exploring its chemical and practical applications.

Interesting facts

Interesting Facts About 6-Ethyltetralin

6-Ethyltetralin, a derivative of tetralin, is an exciting compound that has piqued the interest of both chemists and researchers due to its unique structural characteristics and potential applications. Here are some noteworthy points:

  • Structural Composition: As a polycyclic compound, 6-ethyltetralin is a member of the bicyclic aromatic hydrocarbons, which makes it intriguing for studies related to ring strain and molecular stability.
  • Origins: It can be synthesized through various methods, including the alkylation of tetralin. Such synthesis routes are not only of academic interest but also hold industrial significance.
  • Natural Sources: Compounds with similar structures can be found in certain essential oils, which suggests that 6-ethyltetralin may play a role in the chemistry of natural products.
  • Applications: Its potential applications span various fields, including:
    • As a chemical intermediate in organic synthesis.
    • In the development of new materials with tailored properties.
    • In the study of polycyclic aromatic hydrocarbons and their behavior.
  • Research Potential: Ongoing research aims to explore its behavior under different conditions, shedding light on its reactivity and the potential for new derivatives.
  • Environmental Considerations: Understanding the environmental impact of 6-ethyltetralin is crucial, particularly regarding its biodegradability and interactions within ecosystems.

In conclusion, 6-ethyltetralin is more than just a chemical compound; it embodies a wealth of opportunities for discovery. As scientists continue to delve into its properties and applications, this compound stands as a testament to the complexity and wonder of organic chemistry.

Synonyms
6-Ethyltetraline
22531-20-0
6-ETHYL-1,2,3,4-TETRAHYDRONAPHTHALENE
6-Ethyltetralin
Naphthalene, 6-ethyl-1,2,3,4-tetrahydro-
DTXSID20177046
6-ethyl-1,2,3,4-tetrahydro-naphthalene
RefChem:1073916
SCHEMBL442330
SCHEMBL695095
SCHEMBL2879790
SCHEMBL2879792
SCHEMBL6898460
DTXCID9099537
SCHEMBL30361595
DLHGUEXPTGUBGR-UHFFFAOYSA-N
SBB061515
AKOS006273349
1,2,3,4-tetrahydro-6-ethylnaphthalene
6-Ethyl-1,2,3,4-tetrahydronaphthalene #
DB-219841
ST51047518
InChI=1/C12H16/c1-2-10-7-8-11-5-3-4-6-12(11)9-10/h7-9H,2-6H2,1H