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1,4,6-Trimethyltetralin

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Identification
Molecular formula
C13H18
CAS number
38861-79-1
IUPAC name
1,4,6-trimethyltetralin
State
State

At room temperature, 1,4,6-Trimethyltetralin is in a liquid state.

Melting point (Celsius)
-35.00
Melting point (Kelvin)
238.15
Boiling point (Celsius)
266.00
Boiling point (Kelvin)
539.15
General information
Molecular weight
174.29g/mol
Molar mass
174.2860g/mol
Density
0.9058g/cm3
Appearence

1,4,6-Trimethyltetralin appears as a colorless liquid. It is typically clear and without any suspended particles or coloration, reflecting its purity and specific structure.

Comment on solubility

Solubility of 1,4,6-trimethyltetralin

1,4,6-trimethyltetralin, with its complex structure, presents interesting characteristics regarding its solubility. This compound is generally considered to be:

  • Low Solubility in Water: Due to its hydrophobic nature, 1,4,6-trimethyltetralin has minimal solubility in water. This is primarily attributed to the presence of multiple methyl groups, which reinforce its non-polar characteristics.
  • Soluble in Organic Solvents: It exhibits good solubility in non-polar organic solvents such as hexane and benzene, making it a suitable candidate in various chemical applications.
  • Influence of Temperature: Like many organic compounds, its solubility in organic solvents can increase with temperature, enhancing kinetic energy and allowing for better interaction with solvent molecules.

In summary, the solubility profile of 1,4,6-trimethyltetralin emphasizes its non-polar characteristics, which govern its behavior in different solvent environments. Its limited aqueous solubility juxtaposed with favorable solubility in organic media highlights its unique applications in chemical synthesis and related fields.

Interesting facts

Interesting Facts about 1,4,6-trimethyltetralin

1,4,6-trimethyltetralin is an intriguing organic compound that captures the interest of chemists and researchers alike due to its unique structure and properties. Here are some fascinating points about this compound:

  • Structural Significance: The molecule features a tetralin backbone, which is a bicyclic compound made up of two fused aromatic rings. Its distinct arrangement allows for diverse interactions in chemical reactions.
  • Applications: 1,4,6-trimethyltetralin is utilized in various applications, including its role as a model compound in studying the properties of more complex hydrocarbon mixtures.
  • Synthetic Relevance: It serves as an important building block for synthesizing a wide array of natural products and pharmaceuticals. This includes development in medicinal chemistry where precise modifications can lead to enhanced biological activities.
  • Research Interests: Scientists explore its potential in materials science, as research suggests that compounds like 1,4,6-trimethyltetralin can contribute to the creation of innovative polymers and composite materials.
  • Hydrophobic Characteristics: The non-polar nature of this compound makes it valuable in studies involving hydrophobic interactions, particularly in biochemical processes and environmental chemistry.

In the words of chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." Studying compounds like 1,4,6-trimethyltetralin encourages creativity in chemistry and expands the horizons of what can be achieved through molecular manipulation.

Overall, this compound represents a blend of simplicity and complexity that embodies the beauty of organic chemistry. Its diverse implications make it a captivating subject for both academic and industrial research.

Synonyms
22824-32-4
1,4,6-Trimethyl-1,2,3,4-tetrahydronaphthalene
Naphthalene, 1,2,3,4-tetrahydro-1,4,6-trimethyl-
1,2,3,4-tetrahydro-1,4,6-trimethyl-naphthalene
1,4,6-TRIMETHYLTETRALIN
SCHEMBL18647492
DTXSID20945520
HIACZWPSGFMDRF-UHFFFAOYSA-N
1,4,6-Trimethyl-1,2,3,4-tetrahydronaphthalene #