Skip to main content

4-Methylindane

ADVERTISEMENT
Identification
Molecular formula
C10H12
CAS number
822-95-5
IUPAC name
4-methylindane
State
State

At room temperature, 4-Methylindane exists as a liquid.

Melting point (Celsius)
-30.50
Melting point (Kelvin)
242.65
Boiling point (Celsius)
199.00
Boiling point (Kelvin)
472.15
General information
Molecular weight
132.21g/mol
Molar mass
132.2050g/mol
Density
0.9262g/cm3
Appearence

4-Methylindane is typically a colorless liquid. It may have a slight aromatic odor characteristic of indane derivatives.

Comment on solubility

Solubility of 4-Methylindane

4-Methylindane, with its unique structure, presents interesting characteristics in terms of solubility. Its solubility can be summarized as follows:

  • Insulation in Water: 4-Methylindane is known to be insoluble in water. This is typical for many hydrocarbons, primarily due to their non-polar nature, which does not favor interactions with polar water molecules.
  • Solubility in Organic Solvents: Conversely, this compound exhibits good solubility in a range of organic solvents. Common solvents where it readily dissolves include:
    • Hexane
    • Toluene
    • Acetone
  • Temperature Dependence: The solubility of 4-methylindane in organic solvents can also increase with temperature; hence, higher temperatures often facilitate better dissolution.

In conclusion, while 4-methylindane remains insoluble in water, its compatibility with organic solvents highlights its importance in various chemical processes. Understanding these solubility characteristics can be crucial for applications in both laboratory settings and industrial processes.

Interesting facts

Interesting Facts about 4-Methylindane

4-Methylindane is a fascinating aromatic hydrocarbon that captures the interest of chemists and organic scientists alike. Below are some compelling insights and notable aspects of this compound:

  • Structure and Isomerism: As a derivative of indane, 4-methylindane possesses a unique structure characterized by a fused benzene and cyclopentane ring. The presence of the –CH₃ (methyl) group at the 4-position greatly influences its chemical properties and reactivity.
  • Reactivity: The methyl substitution enhances the electrophilic nature of the compound, making it an interesting candidate for various chemical reactions, including electrophilic aromatic substitution, which is fundamental in organic synthesis.
  • Applications in the Industry: This compound finds use in the production of specialty chemicals and materials, particularly in the formulation of certain polymers and high-performance materials.
  • Research Significance: 4-Methylindane and its derivatives are investigated for potential applications in pharmaceuticals and agrochemicals due to their biological activities. Some studies have suggested that these compounds may exhibit anti-inflammatory and analgesic properties.
  • Historical Context: The synthesis and study of substituted indanes have contributed significantly to the field of organic chemistry, offering insights into reaction mechanisms and molecular interactions.

In conclusion, 4-methylindane serves as a prime example of how simple structural modifications can lead to complex chemical behavior and diverse applications in science and industry. Its study not only enriches our understanding of organic compounds but also opens pathways to innovative discoveries!

Synonyms
4-methyl-2,3-dihydro-1H-indene
4-METHYLINDAN
1H-Indene, 2,3-dihydro-4-methyl-
Indan, 4-methyl-
UNII-2XB2R8T53C
2XB2R8T53C
2,3-dihydro-4-methyl-1H-indene
EINECS 212-524-9
DTXSID7073931
1H-INDENE,2,3-DIHYDRO-4-METHYL
DTXCID7048293
212-524-9
lnnsodhyzxcejp-uhfffaoysa-n
824-22-6
4-Methylindane
2,3-Dihydro-4-methyl-1H-indene; 4-Methylindan
MFCD16300725
AKOS022299860
AS-60069
DB-242083
CS-0153381
NS00038197
Y11654
Q27255751