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1,2-dimethylindane

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Identification
Molecular formula
C11H14
CAS number
605-13-8
IUPAC name
1,2-dimethylindane
State
State

At room temperature, 1,2-dimethylindane is typically in a liquid state.

Melting point (Celsius)
-50.00
Melting point (Kelvin)
223.20
Boiling point (Celsius)
237.50
Boiling point (Kelvin)
510.60
General information
Molecular weight
132.21g/mol
Molar mass
132.2050g/mol
Density
0.9154g/cm3
Appearence

1,2-Dimethylindane is a clear, colorless liquid at room temperature. It can appear slightly oily due to its hydrocarbon nature.

Comment on solubility

Solubility of 1,2-dimethylindane

1,2-dimethylindane is an organic compound known for its unique structure and properties. When it comes to solubility, the following points should be considered:

  • Solvent Compatibility: Due to its relatively non-polar characteristics, 1,2-dimethylindane is generally soluble in non-polar solvents, such as hexane and benzene.
  • Water Solubility: This compound exhibits very low solubility in water, primarily because of its hydrophobic nature.
  • Temperature Influence: Solubility can also be affected by temperature, with higher temperatures often enhancing solubility in organic solvents.

As a general rule, one might say, "Like dissolves like." This maxim highlights why 1,2-dimethylindane's solubility is more favorable in non-polar environments rather than in polar ones like water.

In summary, if you are working with 1,2-dimethylindane, consider using non-polar solvents to achieve effective dissolution while being mindful of its limited solubility in polar solvents.

Interesting facts

Interesting Facts about 1,2-Dimethylindane

1,2-Dimethylindane is a fascinating compound, belonging to the family of indane derivatives. This compound has unique structural characteristics that make it an intriguing subject of study in organic chemistry. Here are some notable points about 1,2-dimethylindane:

  • Substituted Aromatic Hydrocarbon: As a substituted indane, 1,2-dimethylindane exhibits properties typical of aromatic hydrocarbons, such as resonance stability. This structure allows for interesting chemical reactivity.
  • Synthesis Methods: The synthesis of 1,2-dimethylindane can be achieved through various methods, including the Friedel-Crafts reaction or as a product in the alkylation of indane with methyl halides. It's this versatility in synthesis that makes it a valuable compound in organic synthesis.
  • Applications in Research: 1,2-Dimethylindane has garnered interest in the fields of material science and organic electronics. Its distinct properties can lead to potential applications in the development of novel materials.
  • Isomeric Nature: The compound has a unique positional isomer, known as 1,3-dimethylindane, which adds to the complexity and study of indane derivatives. The differences in position significantly affect the physical and chemical properties of these compounds.
  • Chemical Reactivity: The presence of methyl groups at the 1 and 2 positions of the indane framework can influence reactivity patterns, leading to various substitution reactions that are of high interest in synthetic chemistry.

To sum it up, 1,2-dimethylindane is an appealing compound due to its structural nuances and potential applications in various fields. Its continued exploration by chemists can lead to advancements in synthetic methods and innovative uses in material science.

Synonyms
1,2-dimethyl-2,3-dihydro-1H-indene
17057-82-8
1,2-DIMETHYLINDAN
1H-Indene, 2,3-dihydro-1,2-dimethyl-
Indan, 1,2-dimethyl-
2,3-Dihydro-1,2-dimethyl-1H-indene
1H-INDENE,2,3-DIHYDRO-1,2-D
1,2-Dimethylindane
1,2-dimethyl-indane
1,2-dimethylhydrindene
SCHEMBL217130
SCHEMBL410055
SCHEMBL31124279
DTXSID00937786
DIUGYPAVPJILFZ-UHFFFAOYSA-N