Skip to main content

Pinoline

ADVERTISEMENT
Identification
Molecular formula
C12H12N2O
CAS number
20315-68-8
IUPAC name
2H-pyrido[3,4-b]indol-3-ylmethanol
State
State

At room temperature, pinoline is normally in a solid crystalline state.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
363.00
Boiling point (Kelvin)
636.15
General information
Molecular weight
200.25g/mol
Molar mass
200.2470g/mol
Density
1.2230g/cm3
Appearence

Pinoline typically appears as a crystalline solid. It can form colorless to white crystals depending on purity and is often found as a powder.

Comment on solubility

Solubility of 2H-pyrido[3,4-b]indol-3-ylmethanol

The solubility of a compound like 2H-pyrido[3,4-b]indol-3-ylmethanol (C12H12N2O) is a significant factor to consider for its applications in various fields. This compound presents unique characteristics influencing its solubility, primarily due to its organic structure and functional groups.

Factors Affecting Solubility

The solubility can be influenced by several factors:

  • Polarity: Given the presence of hydroxyl (-OH) group, the compound exhibits some polar characteristics, which can enhance its solubility in polar solvents like water.
  • Hydrogen Bonding: The -OH group is capable of forming hydrogen bonds, potentially increasing solubility in suitable solvents.
  • Temperature: As with many organic compounds, temperature variations may affect its solubility; generally, increased temperatures enhance solubility.

Solvent Compatibility

While this compound may be more soluble in certain solvents, it could exhibit limited solubility in:

  • Apolar Solvents: Such as hexane or toluene, due to the lack of polar interactions.
  • Cold Solvents: Lower temperatures may reduce its solubility further, especially in non-polar mediums.

In conclusion, the solubility of 2H-pyrido[3,4-b]indol-3-ylmethanol is a complex interplay of its molecular structure and environmental factors. Understanding its solubility is crucial for its effective utilization in chemical synthesis and pharmaceutical formulations.

Interesting facts

Exploring 2H-pyrido[3,4-b]indol-3-ylmethanol

2H-pyrido[3,4-b]indol-3-ylmethanol is a fascinating compound that belongs to the class of indole-derivative structures. Its unique chemical composition and structure present a myriad of interesting features:

  • Structure and Function: The compound incorporates a pyridine cycle fused with an indole structure, which is pivotal in many biological processes. This blend yields potential pharmacological properties that are of great interest to medicinal chemists.
  • Biological Activity: Compounds with similar indole and pyridine scaffolds have been studied for their various biological activities, including their roles as anti-cancer agents, anti-inflammatory drugs, and neuroprotective agents.
  • Synthesis: The synthesis of 2H-pyrido[3,4-b]indol-3-ylmethanol can be a challenging yet rewarding process. Its preparation often involves multi-step chemical reactions that require keen analytical skills and a thorough understanding of organic chemistry principles.

The structure is often noted for its versatility in the synthesis of new compounds, which can lead to the discovery of novel therapeutic agents. As a result, it garners significant attention in research fields aimed at developing new drugs.

The phrase "in the world of molecules, variety is the spice of life" holds particularly true for 2H-pyrido[3,4-b]indol-3-ylmethanol, illustrating how such complex compounds can be both challenging and rewarding to study. For students and scientists alike, delving into the chemistry of this compound can enhance understanding of indole chemistry and its wider implications in biological systems.