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N,N'-bis(4-chlorophenyl)formamidine

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Identification
Molecular formula
C13H10Cl2N2
CAS number
6780-85-0
IUPAC name
N,N'-bis(4-chlorophenyl)formamidine
State
State
N,N'-bis(4-chlorophenyl)formamidine is a solid at room temperature.
Melting point (Celsius)
163.00
Melting point (Kelvin)
436.15
Boiling point (Celsius)
355.00
Boiling point (Kelvin)
628.15
General information
Molecular weight
267.13g/mol
Molar mass
267.1790g/mol
Density
1.3600g/cm3
Appearence

N,N'-bis(4-chlorophenyl)formamidine typically appears as a crystalline solid. The crystals may be either white or off-white in color, and they possess a characteristic planar structure due to the presence of aromatic rings connected by the formamidine group.

Comment on solubility

Solubility of N,N'-bis(4-chlorophenyl)formamidine

N,N'-bis(4-chlorophenyl)formamidine, with its complex structure, exhibits interesting solubility characteristics that are essential for its applications. Overall, the solubility of this compound can be summarized as follows:

  • Polarity: The compound contains both polar and non-polar components, which can influence its solubility in various solvents.
  • Solvent Compatibility: Generally, N,N'-bis(4-chlorophenyl)formamidine is expected to be soluble in:
    • Polar solvents such as methanol and dimethyl sulfoxide (DMSO) due to interactions with the polar functional groups.
    • Less soluble in non-polar solvents like hexane and benzene, because of its polar nature.
  • Temperature Influence: Solubility may increase with temperature, enhancing solvation dynamics in polar solvents.

In conclusion, understanding the solubility of N,N'-bis(4-chlorophenyl)formamidine is crucial for maximizing its effectiveness in chemical reactions and applications. Its solubility properties must be taken into account when selecting solvents for laboratory procedures and production processes.

Interesting facts

Interesting Facts about N,N'-bis(4-chlorophenyl)formamidine

N,N'-bis(4-chlorophenyl)formamidine is a fascinating organic compound that holds significance in various fields of chemistry and material science. Here are some notable highlights:

  • Structural Insight: This compound is characterized by its unique structure, which features two 4-chlorophenyl groups attached to a formamidine backbone. The presence of the chlorinated phenyl rings enhances its chemical properties, making it an attractive target for research.
  • Pharmaceutical Relevance: Compounds like N,N'-bis(4-chlorophenyl)formamidine have been studied for their potential bioactivity. Their structure can lead to the development of new drug candidates, particularly in the field of anti-cancer and anti-inflammatory therapies.
  • Complexity and Reactivity: The compound's functional groups contribute to its reactivity profile, allowing for interesting chemical transformations. This reactivity is critical for synthetic chemists aiming to create new materials or modify existing compounds.
  • Environmental Considerations: The chlorinated derivatives often present unique challenges and opportunities in environmental science. Understanding their behavior and degradation pathways can lead to better management practices for industrial and pharmaceutical waste.
  • Analytical Techniques: Investigating such compounds involves sophisticated analytical methods. Techniques like NMR spectroscopy, mass spectrometry, and X-ray crystallography are pivotal in elucidating their structure and properties.

In summary, N,N'-bis(4-chlorophenyl)formamidine is more than just a compound; it symbolizes the intricate relationship between structure and function in chemistry. As researchers continue to explore its properties and applications, it may pave the way for advances in multiple scientific disciplines.

Synonyms
N,N'-bis-(4-Chlorophenyl)formamidine
2032-24-8
DTXSID90274571
DTXCID20226043
jkrstgffpvkiqn-uhfffaoysa-n
NSC55503
SCHEMBL3342224
NSC-55503