Propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate

Identification

Molecular formula

C₂₀H₃₀N₂O₃

CAS number

159350-66-2

IUPAC name

propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate

State

At room temperature, propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate is usually in a solid state.

Melting point (Celsius)

102.50

Melting point (Kelvin)

375.65

Boiling point (Celsius)

459.50

Boiling point (Kelvin)

732.65

General information

Molecular weight

346.45g/mol

Molar mass

346.4520g/mol

Density

1.1243g/cm³

Appearence

Propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate typically appears as a white to off-white crystalline solid.

Comment on solubility

Solubility of Propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate

The solubility of propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate is influenced by several factors inherent to its molecular structure. This compound, with its complex arrangement, behaves differently in various solvents:

Polar Solvents: Solubility in polar solvents such as water is generally low due to the hydrophobic nature of the organic components, which can hinder interaction with water molecules.
Non-Polar Solvents: On the other hand, propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate tends to show better solubility in non-polar organic solvents such as hexane or chloroform, where its hydrophobic characteristics align better.
Temperature Effects: Temperature also plays a significant role; increasing the temperature typically enhances solubility for many organic compounds, allowing for greater dissolution rates.

In summary, while this compound may not be readily soluble in water, its solubility in non-polar solvents presents a favorable alternative. As one researcher noted, "the solubility of a compound can often predict its behavior in biological systems and reactions," highlighting the importance of understanding solubility in the study of chemical compounds.

Interesting facts

Interesting Facts about Propyl 3,5-Dimethyl-4-[2-(1-Piperidyl)propanoylamino]benzoate

Propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate is a fascinating compound that showcases the beauty of organic chemistry and its application in medicinal chemistry. Here are some engaging details about this compound:

Structural Complexity: This compound features multiple functional groups which contribute to its unique properties. The presence of a piperidine ring adds a nitrogen atom that can significantly influence its biological activity.
Potential Therapeutic Uses: Compounds with structural similarities to this molecule may serve as important candidates in drug development, particularly in treating neurological disorders due to their ability to cross the blood-brain barrier.
Mechanism of Action: The distinct arrangement of methyl groups and the benzoate moiety can influence the way this compound interacts with biological targets, possibly impacting receptor bindings and signaling pathways.
Synthetic Pathways: The synthesis of this compound might involve a series of intricate reactions that showcase the ingenuity of organic synthesis, further emphasizing the importance of reaction conditions and reagent selection.
Research Potential: Due to its unique structure, this compound can be a valuable subject in the study of structure-activity relationships (SAR) which helps in identifying how changes in structure can enhance therapeutic efficacy.

In summary, Propyl 3,5-dimethyl-4-[2-(1-piperidyl)propanoylamino]benzoate highlights the intricate relationship between molecular structure and function. It serves as a reminder of the potential that organic compounds hold in advancing medicine and enhancing our understanding of chemical interactions.