3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole

Identification

Molecular formula

C₁₄H₁₆N₂

CAS number

IUPAC name

3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole

State

At room temperature, 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole is a solid.

Melting point (Celsius)

160.00

Melting point (Kelvin)

433.15

Boiling point (Celsius)

305.00

Boiling point (Kelvin)

578.15

General information

Molecular weight

212.28g/mol

Molar mass

212.2840g/mol

Density

1.1234g/cm³

Appearence

The compound 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole typically appears as a solid at room temperature. Its color can vary depending on the specific conditions and purity but generally presents as a white to off-white crystalline powder.

Comment on solubility

Solubility of 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole

The solubility of 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole can be characterized by several intriguing factors:

Polarity: The presence of multiple functional groups influences its polarity, which directly impacts its solubility in various solvents.
Solvent Interaction: This compound is likely to exhibit differences in solubility in polar versus non-polar solvents, potentially being more soluble in organic solvents like dichloromethane rather than water.
Hydrogen Bonding: The ability to form hydrogen bonds with other molecules can enhance its solubility in certain environments.
Temperature Effects: Like many organic compounds, its solubility may increase with temperature, allowing for greater dissolution in solvents at elevated temperatures.

In conclusion, while specific solubility data for 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole may not be readily available, the interplay of its structural characteristics and the nature of the solvent play significant roles in determining solubility. Understanding these factors is crucial for practical applications and further research.

Interesting facts

Exploring 3,6-Dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole

3,6-Dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole is a fascinating compound that belongs to the class of heterocyclic organic compounds. Its unique structure, featuring a fused azepine and indole moiety, allows for a diverse range of applications in various fields:

Pharmaceutical Potential: This compound is of particular interest in medicinal chemistry. Compounds that contain indole structures are often evaluated for their pharmacological activities, including anti-cancer, anti-inflammatory, and neuroprotective properties.
Structural Versatility: The presence of the dimethyl substituents increases the versatility of its reactions, facilitating the development of derivatives with tailored biological activities.
Research Applications: Its unique bicyclic framework makes it a suitable candidate for research in organic synthesis and drug discovery, allowing scientists to explore new synthetic routes and biological assays.
Natural Product Mimicry: Given that many natural products exhibit complex alkaloid structures, the synthesis and study of 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole may mimic or enhance certain biological processes found in nature.

As with many heterocycles, the interactions with biological systems can be quite intricate. Such compounds challenge researchers to delve deeper into understanding their mechanisms of action and potential therapeutic uses. The study of 3,6-dimethyl-1,2,4,5-tetrahydroazepino[4,5-b]indole not only contributes to the field of organic chemistry but also helps pave the way for innovative solutions in healthcare.

In summary: The exploration of this compound encapsulates the intersection of synthetic chemistry and biological application, highlighting the importance of structural diversity in discovering new medicinal therapies.