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1,2-bis[(4-chlorophenyl)methyleneamino]guanidine

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Identification
Molecular formula
C15H12Cl2N4
CAS number
Not available
IUPAC name
1,2-bis[(4-chlorophenyl)methyleneamino]guanidine
State
State

The compound is commonly in a solid state at room temperature. It does not dissolve readily in water, but it might have some solubility in organic solvents depending on its structure and modifications.

Melting point (Celsius)
218.00
Melting point (Kelvin)
491.15
Boiling point (Celsius)
480.00
Boiling point (Kelvin)
753.15
General information
Molecular weight
280.14g/mol
Molar mass
280.1390g/mol
Density
1.3500g/cm3
Appearence

The compound is typically a solid at room temperature. It consists of crystalline particles that are generally white or off-white in color. The presence of chlorine atoms in the structure might impart a slightly more intense hue, depending on the specific form and purity level of the compound.

Comment on solubility

Solubility of 1,2-bis[(4-chlorophenyl)methyleneamino]guanidine

The solubility of 1,2-bis[(4-chlorophenyl)methyleneamino]guanidine can be influenced by various factors, including the compound's molecular structure and the nature of the solvent used. Understanding its solubility characteristics is essential for applications in chemical synthesis and formulation processes.

Factors Affecting Solubility:

  • Polarity: The presence of polar functional groups in the compound can enhance interactions with polar solvents. However, the aromatic rings may hinder overall polarity.
  • Temperature: As temperature increases, solubility generally increases for many solid compounds, making high temperatures a potential method to improve solubility.
  • pH Levels: Changes in pH can drastically affect the ionic state of amine-based compounds, thus altering solubility in aqueous solutions.

In the context of solubility, it is important to note that:

  • The compound may exhibit limited solubility in common organic solvents.
  • It may be more soluble in polar solvents compared to non-polar ones.

As a general observation, many guanidine derivatives, such as this one, may have low aqueous solubility but can dissolve more readily in organic solvents. This feature necessitates careful consideration when selecting solvents for reactions or applications.

Interesting facts

Interesting Facts about 1,2-bis[(4-chlorophenyl)methyleneamino]guanidine

1,2-bis[(4-chlorophenyl)methyleneamino]guanidine, a complex organic compound, is of significant interest in the field of medicinal and organic chemistry. This compound possesses various intriguing characteristics and applications that warrant further exploration.

Key Features

  • Structure: The compound showcases a unique guanidine backbone that is substituted with two 4-chlorophenyl groups. This arrangement contributes to its interesting chemical behavior.
  • Biological Activity: Studies suggest that derivatives of guanidine compounds can exhibit a range of activities, including antimicrobial, anti-inflammatory, and even potential antitumor properties.
  • Mechanism of Action: Guanidine-related compounds often interact with biological pathways by mimicking natural substrates, hence allowing them to influence various cellular processes.
  • Synthetic Pathways: The synthesis of this compound involves intricate organic reactions, making it a point of study for chemists interested in synthetic methodologies and reaction mechanisms.

Applications and Research

This compound opens several avenues for research and applications:

  • Drug Development: Owing to its biological activities, 1,2-bis[(4-chlorophenyl)methyleneamino]guanidine could serve as a lead compound in the development of new pharmaceutical agents.
  • Material Science: Its unique molecular structure might offer valuable insights into designing novel materials that possess specific electronic or photonic properties.

Conclusion

In summary, 1,2-bis[(4-chlorophenyl)methyleneamino]guanidine represents a fascinating molecule for both research and application in various scientific fields. As scientists continue to uncover its potential, it stands as a testament to the intricate interplay of chemistry, biology, and innovative material science.

Synonyms
Cytostat
Robenidine-d8
Chimcoccid;Khimcoccid
SCHEMBL571510
orb1705474
SCHEMBL6729906
1173149-51-3
ABA87551
YWB14951
Hydrazinecarbohydrazonamide, N',2-bis[(4-chlorophenyl)methylene]-