1-phenyl-3-(2-pyridylamino)propan-1-ol

Identification

Molecular formula

C₁₄H₁₆N₂O

CAS number

5470-52-6

IUPAC name

1-phenyl-3-(2-pyridylamino)propan-1-ol

State

The compound is in a solid state at room temperature. It exhibits crystalline features which might be useful for identification purposes based on its visual appearance and ability to form distinct crystals under certain conditions.

Melting point (Celsius)

94.50

Melting point (Kelvin)

367.65

Boiling point (Celsius)

221.50

Boiling point (Kelvin)

494.65

General information

Molecular weight

228.29g/mol

Molar mass

228.2920g/mol

Density

1.1790g/cm³

Appearence

This compound appears as a white to off-white crystalline solid. Its crystalline nature may affect its solubility in various solvents, and the structure can exhibit slight variations based on conditions such as purity and temperature.

Comment on solubility

Solubility of 1-phenyl-3-(2-pyridylamino)propan-1-ol

The solubility of 1-phenyl-3-(2-pyridylamino)propan-1-ol can be influenced by various factors related to its molecular structure. This compound, characterized by both hydrophobic phenyl groups and hydrophilic amino functionalities, exhibits varied solubility behaviors:

Solvent Polarities: Generally, this compound is more soluble in polar solvents (e.g., water, methanol) due to the presence of the amino group.
Hydrogen Bonding: The amino group can engage in hydrogen bonding, enhancing solubility in water.
pH Sensitivity: Its solubility may also change with pH variations, particularly if protonation of the amino group occurs, making it more soluble at lower pH levels.

It is important to note that solubility is not a fixed property, but rather a dynamic equilibrium affected by temperature, concentration, and the presence of other solutes. In summary, while 1-phenyl-3-(2-pyridylamino)propan-1-ol leans towards increased solubility in polar environments, specific conditions can significantly alter its behavior.

Interesting facts

Exploring 1-Phenyl-3-(2-Pyridylamino)propan-1-ol

1-Phenyl-3-(2-pyridylamino)propan-1-ol is a fascinating compound that showcases the intricate world of organic chemistry. Here are some engaging facts about this compound:

Structural Diversity: This compound features a unique structure with both a phenyl group and a pyridylamino group attached to a propanol backbone. This kind of structural diversity often leads to interesting interactions in biological systems.
Potential Biological Activity: Compounds with both amino and alcohol functionalities may exhibit significant biological activities. 1-Phenyl-3-(2-pyridylamino)propan-1-ol could potentially serve as a lead compound in drug discovery, especially in the fields of neuropharmacology and medicinal chemistry.
Application in Synthesis: It may also play an important role as an intermediate in the synthesis of other complex organic molecules, including pharmaceuticals and agrochemicals, making it a compound of interest for synthetic chemists.
Interactions with Biological Targets: Due to its ability to form hydrogen bonds, this compound can interact with various biological targets, potentially influencing their functions. Understanding these interactions can lead to the development of new therapeutic agents.
Spectroscopic Analysis: Chemists can utilize techniques such as NMR and IR spectroscopy to study this compound. These methods are essential for understanding the compound's molecular dynamics, conformational preferences, and interaction mechanisms.

In summary, 1-Phenyl-3-(2-pyridylamino)propan-1-ol is not just another organic molecule; it represents a gateway to understanding complex chemical interactions, potential medicinal applications, and innovative synthetic pathways. As research in this area progresses, this compound may reveal even more exciting properties and uses in the scientific community.