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2-Phenyl-3,1-benzoxazepine

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Identification
Molecular formula
C15H11NO
CAS number
49669-57-2
IUPAC name
2-phenyl-3,1-benzoxazepine
State
State
At room temperature, 2-Phenyl-3,1-benzoxazepine is typically found in a solid state.
Melting point (Celsius)
67.00
Melting point (Kelvin)
340.20
Boiling point (Celsius)
455.20
Boiling point (Kelvin)
728.40
General information
Molecular weight
223.27g/mol
Molar mass
223.2700g/mol
Density
1.1524g/cm3
Appearence

2-Phenyl-3,1-benzoxazepine appears as a crystalline solid, which may vary in color from white to slightly off-white. It is often prepared for research purposes and can be observed to form distinct shapes depending on the crystallization process.

Comment on solubility

Solubility of 2-Phenyl-3,1-benzoxazepine

2-Phenyl-3,1-benzoxazepine, a compound characterized by its fused ring structure, exhibits interesting solubility properties that can influence its application in various fields. Consider the following aspects regarding its solubility:

  • Polarity: The solubility of 2-phenyl-3,1-benzoxazepine is largely dependent on its polarity. Due to its aromatic ring system, it demonstrates moderate polarity, making it soluble in some organic solvents.
  • Solvent Interaction: This compound is typically more soluble in polar aprotic solvents like dimethyl sulfoxide (DMSO) and dimethylformamide (DMF), while being less soluble in non-polar solvents.
  • Temperature Dependence: Solubility can increase with temperature, which is a common trait among many organic compounds. It is beneficial to consider the effects of temperature when attempting to dissolve this compound.

In practical terms, you might find that:

  • For synthesis: Selecting the right solvent can significantly enhance the reaction efficiency.
  • For extraction: Understanding its solubility properties can guide the optimal conditions for purification processes.

Overall, the solubility of 2-phenyl-3,1-benzoxazepine is a key factor in its usability, and careful consideration of solvent choice and temperature can yield favorable results in various applications.

Interesting facts

Exploring 2-Phenyl-3,1-benzoxazepine

2-Phenyl-3,1-benzoxazepine is a fascinating compound belonging to the class of benzoxazepines, which are known for their unique structural characteristics and potential biological activities. Here are some intriguing insights about this compound:

  • Chemical Structure: This compound features a seven-membered ring which contains both oxygen and nitrogen atoms, contributing to its reactivity and the nature of its interactions with other molecules.
  • Biological Relevance: Compounds like 2-phenyl-3,1-benzoxazepine have been investigated for their pharmacological properties. Many benzoxazepines exhibit various biological activities including antidepressant and anxiolytic effects.
  • Potential Applications: Due to its structural complexity, 2-phenyl-3,1-benzoxazepine may serve as a valuable scaffold in medicinal chemistry for the development of new therapeutic agents.
  • Research Interest: The synthesis and functionalization of benzoxazepines are of significant interest in the field of organic chemistry, prompting researchers to explore new synthetic methodologies and derivatives.

As stated by leading chemists, "The journey of discovery in organic chemistry often leads to unexpected benefits, where one compound can lead to multiple therapeutic insights." The study of compounds such as 2-phenyl-3,1-benzoxazepine showcases how comprehensive research can unveil new properties and applications, thereby enhancing our understanding of chemical interactions in biological systems.

In conclusion, 2-phenyl-3,1-benzoxazepine represents an illustrative example of how intricate chemistry can have profound implications in various fields, from pharmaceuticals to the basic understanding of molecular interactions. Its exploration could pave the way for innovative solutions in therapeutic developments.

Synonyms
2-PHENYL-3,1-BENZOXAZEPINE
14300-21-1
3,1-Benzoxazepine, 2-phenyl-
2-Phenyl-3,1-benzoxazepine #
DTXSID50162283
QUXWLCQSCONIQP-UHFFFAOYSA-N