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2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium chloride

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Identification
Molecular formula
C21H28ClNO2
CAS number
Not Available
IUPAC name
2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium;chloride
State
State

At room temperature, 2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium chloride exists as a solid. It is generally stored in a dry environment to prevent degradation.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
255.00
Boiling point (Kelvin)
528.15
General information
Molecular weight
370.92g/mol
Molar mass
370.9180g/mol
Density
1.2330g/cm3
Appearence

The compound typically appears as a white to off-white solid. It is often found in powder or crystalline form and dissolves in water to form a clear solution.

Comment on solubility

Solubility of 2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium;chloride

The solubility of 2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium;chloride is a pivotal factor in its application and behavior in various chemical scenarios. This compound exhibits a few intriguing solubility characteristics:

  • Generally, it shows good solubility in polar solvents such as water, methanol, and ethanol due to the presence of the quaternary ammonium structure.
  • Its solubility is significantly influenced by the bulky dibenzyl group, which can create a sterically hindered environment, impacting interactions with solvent molecules.
  • In non-polar solvents, solubility may be limited, showcasing a hydrophilic-lipophilic balance that must be carefully considered in formulations.

Therefore, understanding these solubility patterns is vital for leveraging its properties in both industrial and laboratory settings. As the saying goes, “like dissolves like,” and for 2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium;chloride, this holds true, emphasizing the importance of solvent choice in achieving desired dissolution outcomes.

Interesting facts

Interesting Facts about 2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium Chloride

This intriguing compound belongs to a class of compounds known as cationic salts, characterized by their unique chemical structure that incorporates both a piperidine ring and a dioxolane moiety. Here are some fascinating insights into this compound:

  • Functional Versatility: The presence of the piperidine ring provides this compound with potential applications in medicinal chemistry, particularly in the development of new drugs due to its ability to act as a versatile building block.
  • Stability Considerations: The dioxolane component contributes to the stability and solubility characteristics of the compound, making it a candidate for use in various chemical reactions and syntheses.
  • Biological Activity: Compounds like this often exhibit a range of biological properties, showing promise in the research of pharmaceuticals targeting the central nervous system, thanks to the piperidine unit.
  • Ion Exchange: Being a quaternary ammonium salt, it has interesting ion-exchange capabilities, which could be beneficial in material science and catalysis.
  • Novel Synthesis Methods: The synthesis of this compound can involve innovative pathways, such as the coupling of piperidines with dioxolane derivatives, presenting opportunities for students and researchers to explore synthetic organic chemistry techniques.

As a researcher or student, delving into the properties and potential applications of 2-(2,2-dibenzyl-1,3-dioxolan-4-yl)piperidin-1-ium chloride not only enriches your understanding of cationic compounds but also sparks curiosity for future explorations in chemical innovation!

Synonyms
2,2-Dibenzyl-4-(2-piperidyl)-1,3-dioxolane hydrochloride
3666-67-9
1,3-DIOXOLANE, 2,2-DIBENZYL-4-(2-PIPERIDYL)-, HYDROCHLORIDE