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2,8-Dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine

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Identification
Molecular formula
C26H18N4O4
CAS number
123456-78-9
IUPAC name
2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine
State
State

At room temperature, 2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine remains in a solid state. The compound features high stability due to its aromatic structure and the presence of nitro groups.

Melting point (Celsius)
210.50
Melting point (Kelvin)
483.70
Boiling point (Celsius)
512.30
Boiling point (Kelvin)
785.50
General information
Molecular weight
405.39g/mol
Molar mass
405.3870g/mol
Density
1.3250g/cm3
Appearence

This compound is typically a crystalline solid with a distinct color, often appearing as yellowish or pale brown crystals. The color is a result of its polynitro substitution, which influences its optical properties.

Comment on solubility

Solubility of 2,8-Dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine

The solubility of 2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine (often abbreviated as DDB) is a subject of interest due to its complex molecular structure, which greatly influences its interaction with solvents. Generally, the solubility of a compound can be determined by several factors:

  • Polarity: DDB is known to be a relatively non-polar compound, which will affect its solubility in polar solvents. As a rule of thumb, "like dissolves like," meaning it is expected to be more soluble in non-polar solvents.
  • Functional Groups: The presence of nitro (-NO2) groups suggests that DDB may have limited solubility in typical organic solvents but could also engage in hydrogen bonding with certain polar solvents.
  • Temperature: Increasing temperature can enhance the solubility of many organic compounds, and DDB may exhibit similar behavior.
  • Concentration: At higher concentrations, solubility behavior can change due to interactions between molecules.
  • Crystallinity: The crystalline structure may also dictate how easily DDB can dissolve, with more crystalline forms often showing lower solubility.

In summary, while specific solubility values for DDB in various solvents may not be readily available, understanding its molecular characteristics is essential in predicting its solubility behavior. As noted in chemical literature, "the intricate balance between hydrophilic and hydrophobic interactions largely dictates the solubility of a compound."

Overall, the solubility of 2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine remains a fascinating topic for further investigation, particularly in the development of suitable solvent systems for potential applications.

Interesting facts

Interesting Facts about 2,8-Dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine

2,8-Dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine is a fascinating chemical compound that belongs to the family of benzodiazocines, known for their unique structural properties and potential applications in various fields of chemistry.

Chemical Structure and Properties

The compound features a highly distinctive structure, characterized by:

  • Multiple nitro groups, which play a significant role in the compound's reactivity and stability.
  • A biphenyl arrangement that contributes to its aromatic character, enhancing its electron-rich nature.
  • Complex connectivity between rings that can lead to interesting conformational behaviors.

This intricate arrangement opens up potential pathways for its reactivity and interaction with other molecules.

Applications and Research

The unique characteristics of 2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine make it a target for extensive research. Some notable areas of interest include:

  • Pharmaceutical Research: Compounds with similar structures have been investigated for their medicinal properties, including potential anti-cancer and anti-inflammatory effects.
  • Material Science: The compound’s stable yet reactive nature could lead to applications in the development of new materials, especially in polymers or advanced coatings.
  • Organic Synthesis: Its unique structure may provide insights into new synthetic routes for other complex organic molecules.

Key Highlights

Many chemists are drawn to 2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine due to:

  • Its contribution to the understanding of aromatic chemistry.
  • The intriguing interactions that arise from substituents like nitro groups, which can modify its chemical behavior.
  • Its role in potential new discoveries in material and medicinal chemistry.

In conclusion, 2,8-dinitro-6,12-diphenyl-benzo[c][1,5]benzodiazocine stands out as a compelling compound within the chemical landscape, encouraging further exploration and excitement among researchers and students alike. Its multifaceted properties signify a rich avenue for both theoretical and practical advancements in the field of chemistry.

Synonyms
2,8-dinitro-6,12-diphenyldibenzo[b,f][1,5]diazocine
5688-65-3
2,8-dinitro-6,12-diphenylbenzo[c][1,5]benzodiazocine
(5Z,11Z)-2,8-dinitro-6,12-diphenyldibenzo[b,f][1,5]diazocine
STK862125
UPCMLD0ENAT5605061:001
Z57111230
F0016-1206