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1,3-bis(4-chlorophenyl)isothiourea

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Identification
Molecular formula
C13H10Cl2N2S
CAS number
22884-33-7
IUPAC name
1,3-bis(4-chlorophenyl)isothiourea
State
State

This compound is typically found as a solid at room temperature, specifically in a crystalline powder form.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
420.00
Boiling point (Kelvin)
693.15
General information
Molecular weight
296.20g/mol
Molar mass
296.1710g/mol
Density
1.3704g/cm3
Appearence

1,3-bis(4-chlorophenyl)isothiourea typically appears as a white to off-white crystalline powder. Its crystalline nature gives it a somewhat granular texture, and the appearance may vary slightly depending on the degree of purity.

Comment on solubility

Solubility of 1,3-bis(4-chlorophenyl)isothiourea

1,3-bis(4-chlorophenyl)isothiourea is a compound that presents some intriguing characteristics in terms of solubility. The solubility of this chemical can be influenced by several factors, including:

  • Polarity: The presence of chlorine atoms on the phenyl rings may enhance the overall polarity of the molecule, impacting its interaction with polar solvents.
  • Hydrogen Bonding: Isothiourea groups contain both nitrogen and sulfur, which can engage in hydrogen bonding, potentially affecting solubility in various solvents.
  • Solvent Compatibility: It is generally more soluble in organic solvents compared to water, making it suitable for applications that require organic solvents for dissolution.

In summary, while the exact solubility can vary based on specific solvent conditions, it can be characterized as:

  1. Moderately soluble in organic solvents
  2. Poorly soluble in water

These factors ensure that when handling 1,3-bis(4-chlorophenyl)isothiourea, one must consider its solubility profile carefully to achieve the desired outcomes in chemical applications.

Interesting facts

Interesting Facts about 1,3-bis(4-chlorophenyl)isothiourea

1,3-bis(4-chlorophenyl)isothiourea is a fascinating compound known for its unique structure and diverse applications in the field of chemistry. Here are some intriguing aspects of this compound:

  • Structural Characteristics: The compound features dual 4-chlorophenyl groups attached to a central isothiourea functional group, which contributes to its intriguing chemical reactivity.
  • Medical Applications: This compound has potential implications in medicinal chemistry. Research has indicated that it may exhibit antitumor and antibacterial properties, making it a candidate for further pharmaceutical exploration.
  • Reactive Properties: The isothiourea moiety often participates in nucleophilic reactions, which can lead to the formation of various biologically active derivatives. This property opens doors for its usage in drug development strategies.
  • Synthetic Versatility: 1,3-bis(4-chlorophenyl)isothiourea can be synthesized through various organic reactions, making it an attractive compound for synthetic chemists looking to create tailored derivatives.
  • Environmental Impact: As with many halogen-containing compounds, the use and disposal of 1,3-bis(4-chlorophenyl)isothiourea must be managed carefully to mitigate any environmental risks associated with chlorinated compounds.

In summary, 1,3-bis(4-chlorophenyl)isothiourea stands out not just for its chemical structure, but also for the potential it holds in medicinal and synthetic chemistry applications. As research continues to unfold, this compound may reveal even more exciting properties and uses in various scientific fields.