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2,3-Dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol

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Identification
Molecular formula
C11H15NO2
CAS number
10540-29-1
IUPAC name
2,3-dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol
State
State

At room temperature, 2,3-Dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol exists as a solid. It is commonly stored in a tightly closed container to protect it from moisture.

Melting point (Celsius)
181.00
Melting point (Kelvin)
454.15
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.15
General information
Molecular weight
205.25g/mol
Molar mass
205.2480g/mol
Density
1.2870g/cm3
Appearence

2,3-Dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol typically presents as a crystalline powder. The color may range from white to pale beige, depending on purity and specific crystal form.

Comment on solubility

Solubility of 2,3-Dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol

The solubility of 2,3-dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol is influenced by its unique chemical structure. Understanding this compound's solubility profile can provide essential insights into its potential applications and behaviors in different solvents.

Factors Affecting Solubility

  • Polarity: Due to the presence of hydroxyl groups (-OH), this compound is likely to exhibit increased polar characteristics, enhancing its solubility in polar solvents such as water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvents can significantly improve solubility. The -OH groups serve as hydrogen bond donors and acceptors, enabling interactions that facilitate dissolution.
  • Temperature: Like many organic compounds, the solubility may vary with temperature. Typically, an increase in temperature can enhance solubility for solids in liquids.

However, due to the complex nature of this compound, solubility can vary widely based on the specific solvent used. As a general rule, the solubility framework can be summarized as:

  1. In polar solvents, expect higher solubility.
  2. In non-polar solvents, the solubility will likely be low due to insufficient interactions.

To conclude, the solubility of 2,3-dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol serves as an intriguing case for study, primarily influenced by its polar functional groups and ability to engage in hydrogen bonding. Understanding this solubility behavior is vital for its practical usage in various chemical applications.

Interesting facts

Fascinating Insights into 2,3-Dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol

2,3-Dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol is an intriguing organic compound that belongs to the isoquinoline family. Its unique structure offers numerous opportunities for exploration in the field of chemistry.

Key Features:

  • Diverse Applications: This compound has potential applications in pharmaceuticals, particularly in the development of therapeutic agents due to its structural attributes.
  • Biological Importance: Isoquinoline derivatives are known to exhibit a wide range of biological activities, encompassing anti-inflammatory, analgesic, and antimicrobial properties.
  • Research Interest: The study of this compound opens up discussions around its role in the synthesis of other complex molecules, serving as a building block in medicinal chemistry.

Additionally, the presence of a dihydroisoquinoline structure often indicates the compound may undergo various chemical reactions, making it a prime candidate for investigating reactivity patterns in organic synthesis.

Exciting Possibilities:

This compound is just one example of how intricate organic chemistry can be, providing insight into both the synthesis of novel substances and the exploration of existing chemical libraries. With ongoing research, the potential of 2,3-dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol in drug development and biological research may yield groundbreaking discoveries.

In summary, 2,3-dimethyl-3,4-dihydroisoquinolin-2-ium-6,7-diol is not just a chemical formula; it embodies the intersection of complexity and utility in modern chemistry, awaiting further exploration and application.