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3-(p-Tolyl)azetidine

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Identification
Molecular formula
C10H13N
CAS number
1196-71-0
IUPAC name
3-(p-tolyl)azetidine
State
State

At room temperature, 3-(p-Tolyl)azetidine is in a liquid state. It is used in various chemical synthesis processes and research applications.

Melting point (Celsius)
-31.00
Melting point (Kelvin)
242.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
147.22g/mol
Molar mass
147.2220g/mol
Density
0.9840g/cm3
Appearence

3-(p-Tolyl)azetidine is typically a colorless liquid. It may also appear as a pale yellow liquid depending on purity and storage conditions.

Comment on solubility

Solubility of 3-(p-tolyl)azetidine

The solubility of 3-(p-tolyl)azetidine can be influenced by various factors, including its chemical structure and the solvent used. Here’s what to consider regarding its solubility:

  • Polarity: 3-(p-tolyl)azetidine contains a hydrophobic p-tolyl group, which may limit its solubility in polar solvents such as water.
  • Solvent Compatibility: It tends to dissolve better in non-polar solvents like hexane or chloroform, highlighting the principle of "like dissolves like."
  • Temperature Influence: Increasing temperature might enhance solubility in organic solvents due to increased molecular motion, allowing for better interaction.

In summary, while 3-(p-tolyl)azetidine may show limited solubility in polar solvents, its solubility improves substantially in non-polar organic solvents. Understanding these solubility characteristics is crucial for its practical applications in synthesis and formulation.

Interesting facts

Interesting Facts about 3-(p-Tolyl)azetidine

3-(p-Tolyl)azetidine is a fascinating compound that belongs to the class of azetidines, a group of five-membered nitrogen-containing heterocycles. Known for their unique structural and electronic properties, azetidines have garnered significant interest in organic chemistry and medicinal research. Here are some compelling aspects of this compound:

  • Structural Significance: The presence of the p-tolyl group enhances the overall stability of the azetidine ring, making it a subject of study for chemists interested in the manipulation of ring strain and reactivity.
  • Applications in Drug Design: Compounds like 3-(p-tolyl)azetidine serve as valuable building blocks in the synthesis of pharmaceuticals. Their structural framework can lead to the development of new therapeutics with potential bioactivity.
  • Isomerism: The compound exhibits stereoisomerism, which is crucial for understanding its biological activity. Different stereoisomers can interact variably with biological systems, highlighting the importance of chiral resolution in drug development.
  • Reactivity: The nitrogen atom in the azetidine ring can participate in various chemical reactions, including nucleophilic substitutions and ring-opening reactions, making this compound of interest to synthetic chemists.
  • Historical Context: Azetidines have a rich history in organic synthesis dating back to the early 20th century, and their study has paved the way for various advancements in both organic chemistry and material science.

This compound exemplifies the intricate relationship between structure and function in chemistry. As we delve deeper into the properties and applications of 3-(p-tolyl)azetidine, it becomes clear that understanding such compounds is essential for breakthroughs in synthetic methodologies and therapeutic developments.

Synonyms
AZETIDINE, 3-p-TOLYL-
3-p-Tolylazetidine
7215-06-7
L 2362
BRN 1424151
DTXSID30222475
5-20-06-00367 (Beilstein Handbook Reference)
DTXCID30144966
3-(p-tolyl)azetidine
3-(4-methylphenyl)azetidine
SCHEMBL16994772
GS0567
MFCD01665447
AKOS006359559
SY267182
EN300-1827611