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(2R,3S)-2,3-diphenylaziridine

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Identification
Molecular formula
C14H13N
CAS number
34204-35-6
IUPAC name
(2R,3S)-2,3-diphenylaziridine
State
State
At room temperature, (2R,3S)-2,3-diphenylaziridine is a solid, indicating its stability and non-volatility under normal conditions.
Melting point (Celsius)
49.00
Melting point (Kelvin)
322.15
Boiling point (Celsius)
321.30
Boiling point (Kelvin)
594.45
General information
Molecular weight
195.26g/mol
Molar mass
195.2610g/mol
Density
1.1250g/cm3
Appearence
This compound appears as a white solid, comprised of crystalline or powder form. It may exhibit a slight odor characteristic of aromatic compounds.
Comment on solubility

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

(2R,3S)-2,3-diphenylaziridine, a chiral compound, presents an intriguing case for solubility analysis due to its unique structure and the presence of aromatic groups. The solubility of this compound can be influenced by several factors:

  • Solvent Polarity: Given its hydrophobic aromatic rings, (2R,3S)-2,3-diphenylaziridine is likely to have low solubility in polar solvents like water.
  • Non-Polar Solvents: It may show better solubility in non-polar or slightly polar organic solvents such as benzene or toluene.
  • Temperature Effects: Increasing the temperature can enhance solubility due to increased molecular motion, allowing for better interactions with the solvent.

As a general rule, the solubility of organic compounds can often be predicted using the principle of "like dissolves like." Therefore, one might expect (2R,3S)-2,3-diphenylaziridine to be more soluble in non-polar frameworks compared to polar environments.

In practical terms, understanding the solubility characteristics of (2R,3S)-2,3-diphenylaziridine is essential for its application in various chemical processes, including synthesis and purification methods. As a general observation, solubility is a critical parameter that affects not only the reaction dynamics but also the stability and reactivity of the compound in solution.

Interesting facts

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

(2R,3S)-2,3-diphenylaziridine is a fascinating compound due to its unique structure and potential applications in various fields of chemistry. Here are some key points that highlight its significance:

  • Stereochemistry: This compound features a chiral center at both the 2 and 3 positions, imparting it with optical activity. The (2R,3S) designation indicates the specific configuration of the molecule, which can lead to variations in biological activity and reactivity.
  • Reactivity: The aziridine ring is known for its ring strain, making it a versatile reactant in nucleophilic substitution reactions. This property enables it to participate in the synthesis of more complex organic compounds.
  • Applications: Compounds like (2R,3S)-2,3-diphenylaziridine are significant in medicinal chemistry. They can serve as lead compounds in the development of pharmaceuticals, particularly in creating targeted therapies.
  • Biological Potential: Research shows that aziridines can exhibit interesting biological activities. Studies on this compound may yield insights into its potential as an antimicrobial or anticancer agent.
  • Studying Mechanisms: Understanding the reactivity of (2R,3S)-2,3-diphenylaziridine could help chemists develop new methodologies in organic synthesis, advancing the field of synthetic organic chemistry.

As we delve deeper into the properties and applications of this compound, we may uncover more about its capabilities and roles in science. The study of (2R,3S)-2,3-diphenylaziridine continues to be a promising area for research, offering a glimpse into the intricate world of chemical compounds.

Synonyms
cis-2,3-Diphenylaziridine
cis-Stilbenimine
1605-06-7
cis-Stilbene imine
NSC 42447
CCRIS 2078
BRN 0082734
AZIRIDINE, 2,3-DIPHENYL-, cis-
Aziridine,3-diphenyl-, cis-
SCHEMBL10376420
DTXSID901312384
(2R,3S)-2,3-Diphenyl-aziridine
NSC42447
NSC-42447
Rel-(2S,3R)-2,3-diphenylaziridine