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1-tert-butyl-3,5-diethylbenzene

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Identification
Molecular formula
C14H22
CAS number
7772-85-0
IUPAC name
1-tert-butyl-3,5-diethyl-benzene
State
State

At room temperature, 1-tert-butyl-3,5-diethylbenzene exists as a liquid. Its aromatic ring and alkyl substitutions prevent it from having a higher melting point which would make it solid at room temperature.

Melting point (Celsius)
-46.00
Melting point (Kelvin)
227.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
204.36g/mol
Molar mass
204.3610g/mol
Density
0.8633g/cm3
Appearence

1-tert-butyl-3,5-diethylbenzene appears as a colorless to pale yellow liquid. It is typically clear and has an aromatic odor typical of alkyl-benzenes. The compound is used in organic synthesis and as an intermediate in various chemical processes.

Comment on solubility

Solubility of 1-tert-butyl-3,5-diethyl-benzene

1-tert-butyl-3,5-diethyl-benzene, a polyalkylated aromatic compound, exhibits notable solubility characteristics that are important for its applications in various chemical processes. Its solubility can be influenced by several factors, including:

  • Polarity: The presence of bulky tert-butyl and ethyl groups contributes to its overall nonpolar nature.
  • Solubility in Organic Solvents: This compound is generally insoluble in water due to its hydrophobic character, but it shows good solubility in organic solvents such as:
    • Hexane
    • Toluene
    • Diethyl ether
    • Chloroform
  • Temperature Effects: As with many organic compounds, solubility may increase with temperature, allowing for better dissolution in organic media at elevated temperatures.

In summary, the solubility profile of 1-tert-butyl-3,5-diethyl-benzene highlights its compatibility with nonpolar solvents and its lack of solubility in polar solvents like water, making it essential for many industrial applications.

Interesting facts

Interesting Facts about 1-tert-butyl-3,5-diethyl-benzene

1-tert-butyl-3,5-diethyl-benzene is a fascinating compound that belongs to the class of organic compounds known as polyalkylated benzenes. Its unique structure consists of a benzene ring with multiple alkyl groups, which significantly alter its physical and chemical properties. Here are some interesting facts about this compound:

  • Structural Versatility: The presence of the tert-butyl and diethyl groups provides a rich avenue for reactivity. This structural versatility can be exploited for various synthetic applications in organic chemistry.
  • Applications in Industry: Compounds like 1-tert-butyl-3,5-diethyl-benzene are often used as precursors in the synthesis of more complex molecules, potentially leading to innovations in pharmaceuticals and dyes.
  • Research Relevance: Its complex structure makes it a subject of interest in studies exploring *sterics* and *electron-donating effects*, which are critical for understanding reaction mechanisms in organic chemistry.
  • Environmental Considerations: As with many organic compounds, studies on the environmental impact and degradation pathways of 1-tert-butyl-3,5-diethyl-benzene offer insights into how we can mitigate pollutants in ecosystems.

Furthermore, the compound's large tert-butyl group can create steric hindrance, which influences its reactivity and interactions with other molecules. As a chemistry student, understanding the implications of *sterics* in compound behavior can deepen your knowledge of organic reactions.

In summary, 1-tert-butyl-3,5-diethyl-benzene not only exemplifies structural intricacies within organic compounds but also serves as a valuable tool in chemical research and application. Exploring its properties can lead to greater insights into the world of organic chemistry.

Synonyms
5-(TERT-BUTYL)-M-CYMENE
29577-19-3
DTXSID10183752
RefChem:101843
DTXCID50106243
1-tert-butyl-3,5-diethylbenzene
1,3-diethyl-5-t-butylbenzene
SCHEMBL9934549
SCHEMBL28354914