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trans-2,3-Diphenylaziridine

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Identification
Molecular formula
C14H13N
CAS number
87262-89-7
IUPAC name
(2R,3R)-2,3-diphenylaziridine
State
State

At room temperature, trans-2,3-Diphenylaziridine is typically a solid. This makes it easier to handle and measure in laboratory settings. The compound remains stable under normal room conditions, but should be kept sealed tightly to avoid moisture absorption or other atmospheric interactions.

Melting point (Celsius)
49.50
Melting point (Kelvin)
322.65
Boiling point (Celsius)
230.80
Boiling point (Kelvin)
503.95
General information
Molecular weight
209.29g/mol
Molar mass
209.2870g/mol
Density
1.1650g/cm3
Appearence

Trans-2,3-Diphenylaziridine appears as a colorless crystalline solid. It may also be encountered in the form of fine, white to off-white powder. The crystalline nature adds a certain sheen to the material, especially under light. It is typically stable when stored in a dry, cool place, away from direct sunlight or heat sources. Proper laboratory handling practices should be used when dealing with the compound to maintain its integrity.

Comment on solubility

Solubility of (2R,3R)-2,3-diphenylaziridine

(2R,3R)-2,3-diphenylaziridine is an intriguing compound with notable solubility characteristics that can affect its applications in various fields. Understanding its solubility can be vital for successful formulation and usage. Here are some key points to consider regarding its solubility:

  • Solvent Specificity: The solubility of (2R,3R)-2,3-diphenylaziridine may vary significantly depending on the solvent used. It tends to be more soluble in organic solvents such as ethanol and acetone.
  • Polarity Influence: Given the non-polar nature of the diphenyl moieties, (2R,3R)-2,3-diphenylaziridine generally shows lower solubility in polar solvents, which may lead to challenges in achieving desired concentrations in highly polar media.
  • Temperature Dependency: Like many organic compounds, its solubility can be affected by temperature; typically, increased temperature enhances solubility, aiding in the dissolution process.
  • Complex Formation: The presence of functional groups may also allow for potential complex formation with other molecules, impacting its effective solubility in certain conditions.

In conclusion, the solubility of (2R,3R)-2,3-diphenylaziridine is a multifaceted aspect that warrants careful consideration in experimental design and industrial applications. As it can be influenced by several factors, understanding these nuances allows for better exploitation of the compound's unique properties.

Interesting facts

Interesting Facts about (2R,3R)-2,3-diphenylaziridine

(2R,3R)-2,3-diphenylaziridine is a fascinating compound that captures the interest of chemists due to its unique structural characteristics and potential applications in various fields. Here are some engaging points about this intriguing aziridine:

  • Unique Structure: Aziridines are known for their three-membered ring structure, which introduces significant strain. This strain often makes them more reactive than other cyclic compounds, allowing for interesting chemistry.
  • Chiral Centers: The (2R,3R) configuration indicates the presence of *stereocenters*, making this compound chiral. Chirality plays a crucial role in pharmaceutical applications, as different enantiomers can exhibit different biological activities.
  • Applications in Synthesis: Aziridines, including (2R,3R)-2,3-diphenylaziridine, are valuable intermediates in organic synthesis. They can serve as key building blocks for synthesizing more complex molecules, particularly in the development of pharmaceuticals.
  • Biological Relevance: Compounds with aziridine structures have been studied for their potential anti-cancer properties. Their reactivity allows them to interact with biological molecules, opening avenues for novel drug design.
  • Potential Catalysts: Researchers are exploring the use of aziridines in catalysis. The strain inherent in the aziridine ring can facilitate various reactions, making them potential candidates for use in asymmetric catalysis.

This compound perfectly exemplifies the intersection of chemistry and pharmacology, showcasing how subtle differences in molecular structure can lead to significant changes in chemical behavior and biological activity.

As Jedlinski once said, "The beauty of chemistry lies in its ability to turn the abstract into the tangible, revealing the mysteries of interaction at the molecular level." Exploring compounds like (2R,3R)-2,3-diphenylaziridine is a step deeper into that revelation.

Synonyms
trans-Stilbene imine
CCRIS 2077
NSC 103863
BRN 3943222
AZIRIDINE, 2,3-DIPHENYL-, trans-
5-20-08-00085 (Beilstein Handbook Reference)
25125-72-8
RefChem:320421
trans-Stilbenimine
cis-Stilbene imine
trans-2,3-Diphenylaziridine
SCHEMBL31146730