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2,3,4,5-tetrahydro-1-benzoxepine

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Identification
Molecular formula
C10H12O
CAS number
3195-37-5
IUPAC name
2,3,4,5-tetrahydro-1-benzoxepine
State
State

At room temperature, 2,3,4,5-tetrahydro-1-benzoxepine is in a liquid state.

Melting point (Celsius)
-23.00
Melting point (Kelvin)
250.15
Boiling point (Celsius)
284.00
Boiling point (Kelvin)
557.15
General information
Molecular weight
134.21g/mol
Molar mass
134.1840g/mol
Density
0.0000g/cm3
Appearence

2,3,4,5-Tetrahydro-1-benzoxepine is typically a colorless liquid.

Comment on solubility

Solubility of 2,3,4,5-tetrahydro-1-benzoxepine

The solubility of 2,3,4,5-tetrahydro-1-benzoxepine is influenced by several factors that are typical for organic compounds. This compound is characterized by its complex bicyclic structure, which impacts its interaction with solvents. Here are some important points to consider:

  • Polarity: Due to the presence of the benzoxepine ring, this compound exhibits moderate polarity, which affects its solubility in different solvents.
  • Solvent Compatibility: 2,3,4,5-tetrahydro-1-benzoxepine is likely to be soluble in organic solvents such as ethanol, methanol, and chloroform, but may have limited solubility in water.
  • Temperature Influence: As with many organic compounds, increasing the temperature can enhance solubility, making it an essential factor during experimentation.
  • Substituent Effects: Modifications to the benzoxepine structure could alter solubility characteristics, indicating that derivatives may have varying levels of solubility.

In summary, understanding the solubility of 2,3,4,5-tetrahydro-1-benzoxepine requires consideration of its polarity, the solvents used, and environmental conditions. As noted, applicable findings suggest that optimal solubility may be achieved using organic solvents at elevated temperatures, which is critical for applications in chemical synthesis and pharmaceutical development.

Interesting facts

Interesting Facts about 2,3,4,5-Tetrahydro-1-benzoxepine

2,3,4,5-Tetrahydro-1-benzoxepine is a fascinating compound with significant implications in the field of chemistry and pharmacology. Here are some intriguing insights about this molecular structure:

  • Unique Structure: The compound features a benzoxepine moiety, which combines the properties of both aromatic and aliphatic systems. This unique structure contributes to its potential reactivity and interaction with biological targets.
  • Pharmaceutical Potential: Compounds containing the benzoxepine framework have been studied for their possible applications in drug development, particularly in the treatment of neurological disorders.
  • Synthetic Challenge: The synthesis of 2,3,4,5-tetrahydro-1-benzoxepine can be an intriguing challenge for chemists. It often involves multi-step procedures that require careful manipulation of reaction conditions and the use of various reagents.
  • Natural Occurrence: While primarily synthesized in the laboratory, derivatives of benzoxepine can also be found in certain natural products, suggesting their potential roles in biological systems and medicinal chemistry.
  • Research Interest: The compound has become a subject of welcome academic inquiry, with studies focused on its pharmacodynamics and potential as a scaffold for designing novel therapeutic agents.

In summary, the study of 2,3,4,5-tetrahydro-1-benzoxepine not only enhances our understanding of complex organic molecules but also opens avenues for groundbreaking research in medicinal chemistry. As one scientist aptly stated, "The boundaries of chemistry are only as limited as our imagination."

Synonyms
6169-78-4
2,3,4,5-TETRAHYDRO-1-BENZOXEPIN
2,3,4,5-Tetrahydro-1-benzoxepine
Homochroman
1-Benzoxepin, 2,3,4,5-tetrahydro-
benzoxepane
SCHEMBL27493
DTXSID20977260
AKOS006372992
2,3,4,5-Tetrahydro-1-benzoxepine #