1,6-dimethylindane
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- Molecular formula
- C11H14
- CAS Number
- 936-08-3
- IUPAC Name
- 1,6-dimethylindane
- Molecular Weight
- 146.22g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.9510g/cm3
- Synonyms
- 1, 6-DIMETHYLINDAN
Identification
Interesting facts
Interesting Facts about 1,6-Dimethylindane
1,6-Dimethylindane is a fascinating organic compound belonging to the family of indanes, which are bicyclic compounds featuring a benzene ring fused to a cyclopentane. Here are some captivating details about this compound:
- Structure & Isomerism: The unique structure of 1,6-dimethylindane consists of two methyl groups attached to the indane framework. This positioning leads to the potential for isomerism, raising intriguing questions about the reactivity and properties of these variants.
- Synthetic Utility: 1,6-Dimethylindane serves as an important building block in organic synthesis. Chemists often utilize compounds like 1,6-dimethylindane to create more complex molecules, paving the way for innovation in materials and pharmaceuticals.
- Applications in Research: This compound has garnered interest in various fields, including medicinal chemistry and materials science. Its structural features may influence biological activity, making it a candidate for drug development.
- Counterparts in Nature: While 1,6-dimethylindane itself may not be widely found in nature, its structural family does play a role in several naturally occurring substances, highlighting the interconnectedness of chemical structures across different domains.
- Reactivity: When subjected to various reactions, 1,6-dimethylindane showcases interesting behavior due to its electron-rich aromatic ring, often participating in electrophilic aromatic substitution reactions.
To sum it up, 1,6-dimethylindane stands out in the realm of organic compounds, primarily due to its structural intricacies and potential applications. As a chemist delves deeper into its properties, new possibilities may arise, making this compound an exciting topic of study.