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1,5,8-Trimethyl-1,2-dihydronaphthalene

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Identification
Molecular formula
C13H16
CAS number
59702-29-5
IUPAC name
1,5,8-trimethyl-1,2-dihydronaphthalene
State
State

At room temperature, 1,5,8-Trimethyl-1,2-dihydronaphthalene is in a liquid state.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.15
Boiling point (Celsius)
262.00
Boiling point (Kelvin)
535.15
General information
Molecular weight
184.29g/mol
Molar mass
184.2860g/mol
Density
0.9367g/cm3
Appearence

1,5,8-Trimethyl-1,2-dihydronaphthalene is typically a colorless liquid when in pure form. It may exhibit a slight yellowish tint under certain conditions due to impurities or degradation.

Comment on solubility

Solubility of 1,5,8-trimethyl-1,2-dihydronaphthalene

1,5,8-trimethyl-1,2-dihydronaphthalene is a fascinating organic compound with distinctive solubility characteristics. The solubility of this compound can be influenced by various factors including:

  • Polarity: The presence of multiple methyl groups can reduce the overall polarity of the compound, making it less soluble in polar solvents such as water.
  • Solvent Type: Generally, 1,5,8-trimethyl-1,2-dihydronaphthalene is expected to be more soluble in non-polar solvents such as hexane or dichloromethane due to its hydrophobic nature.
  • Temperature: Higher temperatures may enhance solubility in organic solvents as they can provide the energy required to overcome intermolecular forces.

As a result, it is often observed that:

  • It has very low solubility in water.
  • It generally shows better solubility in organic solvents.

In practical applications, understanding the solubility behavior of 1,5,8-trimethyl-1,2-dihydronaphthalene is essential for formulations in organic synthesis and product development.

Interesting facts

Interesting Facts about 1,5,8-trimethyl-1,2-dihydronaphthalene

1,5,8-trimethyl-1,2-dihydronaphthalene is a fascinating compound that holds significant interest in both organic chemistry and industrial applications. Here are some intriguing aspects of this compound:

  • Natural Occurrence: This compound can be found in certain essential oils and plant extracts, showcasing its role in the natural world. It is often associated with the aroma and flavor profiles of various plants.
  • Structural Complexity: As a derivative of naphthalene, 1,5,8-trimethyl-1,2-dihydronaphthalene features a unique arrangement of methyl groups, contributing to an intricate molecular structure that can be a topic of study for chemists.
  • Potential Applications: Due to its distinctive chemical properties, this compound has potential uses in fields such as fragrance formulation and synthetic organic chemistry, making it valuable for product development.
  • Isomerism: This compound's structure allows for the possibility of different stereoisomers, which can exhibit varied chemical behavior, adding an interesting layer to its study in stereochemistry.
  • Research Interest: Chemists are often intrigued by compounds like 1,5,8-trimethyl-1,2-dihydronaphthalene, as they serve as model compounds for exploring reactivity patterns and mechanistic pathways in organic reactions.

In summary, the study of 1,5,8-trimethyl-1,2-dihydronaphthalene not only highlights its chemical uniqueness but also opens up avenues for research and application in various scientific fields. As noted by experts, "Compounds like these are gateways to understanding complex chemical interactions and pave the way for innovative uses in technology and industry."

Synonyms
1,5,8-Trimethyl-1,2-dihydronaphthalene
4506-36-9
1,2-DIHYDRO-1,5,8-TRIMETHYLNAPHTHALENE
Naphthalene, 1,2-dihydro-1,5,8-trimethyl-
Y6D44B0088
UNII-Y6D44B0088
yjfozrtwrvnhog-uhfffaoysa-n
1,4,5-TRIMETHYL-5,6-DIHYDRONAPHTHALENE
1,5,8-Trimethyl-1,2-dihydronaphthalene #