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trans-β-Methylstyrene

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Identification
Molecular formula
C9H10
CAS number
766-90-5
IUPAC name
1-methyl-3-styryl-benzene
State
State

At room temperature, trans-β-Methylstyrene is typically a liquid. It is volatile and has a relatively low viscosity.

Melting point (Celsius)
-21.00
Melting point (Kelvin)
252.15
Boiling point (Celsius)
198.20
Boiling point (Kelvin)
471.35
General information
Molecular weight
118.20g/mol
Molar mass
118.1950g/mol
Density
0.9080g/cm3
Appearence

trans-β-Methylstyrene is a colorless liquid with a distinct aromatic odor typical of aromatic hydrocarbons. Its appearance can become slightly yellowish on exposure to light and air.

Comment on solubility

Solubility of 1-methyl-3-styryl-benzene

1-methyl-3-styryl-benzene, a derivative of styrene, exhibits certain characteristics regarding its solubility in different solvents. The solubility of this compound can be described as follows:

  • Nonpolar Solvents: 1-methyl-3-styryl-benzene is generally expected to be soluble in nonpolar solvents due to its hydrocarbon structure. Solvents such as hexane or toluene provide a suitable environment for dissolution.
  • Polar Solvents: This compound shows limited solubility in polar solvents like water or ethanol. The polar molecules struggle to interact effectively with the largely nonpolar character of the aromatic compound's structure.
  • Temperature Effects: The solubility may also be influenced by temperature changes. As a general rule, increasing the temperature tends to enhance the solubility of organic compounds in organic solvents.

In conclusion, the solubility of 1-methyl-3-styryl-benzene is essentially dictated by its nonpolar nature, making it more compatible with organic solvents rather than polar environments. As one could say, "like dissolves like," highlighting the significance of matching the solute's polarity with that of the solvent.

Interesting facts

Interesting Facts about 1-Methyl-3-styryl-benzene

1-Methyl-3-styryl-benzene, often known in the scientific community for its unique structural characteristics, belongs to the family of aromatic hydrocarbons. This compound features both a methyl and a styryl group, which contribute to its intriguing chemical behavior and potential applications.

Key Characteristics:

  • Structural Versatility: The presence of both the methyl and styryl groups allows for interesting interactions with other molecules, making it a subject of study for materials science.
  • Chemical Reactivity: Due to the conjugated double bond within the styryl group, it exhibits enhanced reactivity, particularly in electrophilic substitution reactions, a key consideration for synthetic chemists.
  • Fluorescent Properties: Compounds in the styryl family often display fluorescence, which opens avenues in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices.

Applications in Research:

1-Methyl-3-styryl-benzene is of interest in various fields, including:

  • Organic Synthesis: It can be utilized as a building block for more complex molecules.
  • Medicinal Chemistry: Research into its potential biological activities is ongoing, particularly as a precursor for drug development.
  • Material Science: Its unique properties may contribute to advancements in polymer chemistry.

As scientists delve deeper into the world of 1-methyl-3-styryl-benzene, they uncover more about its potential and versatility. Its diverse applications showcase the importance of aromatic compounds in modern chemistry, revealing a vast landscape of possibilities for innovation and discovery.

Synonyms
SCHEMBL318044
SCHEMBL4660572
SCHEMBL5535307
SCHEMBL27750015