Skip to main content

Chloroxynil

ADVERTISEMENT
Identification
Molecular formula
C13H8Cl2N2O4
CAS number
65731-84-2
IUPAC name
2,4-dichloro-1-(4-nitrophenoxy)benzene;3-(3,4-dichlorophenyl)-1-methoxy-1-methyl-urea
State
State

The compound is typically in a solid state at room temperature.

Melting point (Celsius)
85.00
Melting point (Kelvin)
358.15
Boiling point (Celsius)
331.00
Boiling point (Kelvin)
604.15
General information
Molecular weight
388.10g/mol
Molar mass
388.0960g/mol
Density
1.5500g/cm3
Appearence

The compound appears as a crystalline solid. It can be colorless to white, exhibiting a crystalline texture.

Comment on solubility

Solubility of 2,4-dichloro-1-(4-nitrophenoxy)benzene and 3-(3,4-dichlorophenyl)-1-methoxy-1-methyl-urea

The solubility of organic compounds can vary significantly based on their chemical structure and intermolecular interactions. Let's delve into the solubility characteristics of these two compounds:

2,4-dichloro-1-(4-nitrophenoxy)benzene

This compound, characterized by the presence of both chlorine and nitro groups, exhibits moderate solubility in organic solvents. Here are some key points to consider:

  • Polar vs. Non-Polar: The presence of polar functional groups often enhances solubility in polar solvents.
  • Common Solvents: Generally soluble in organic solvents like ethanol and acetone, but limited solubility in water.
  • Hydrophobic Effects: The chlorinated aromatic component can contribute to reduced solubility in aqueous environments due to its hydrophobic character.

3-(3,4-dichlorophenyl)-1-methoxy-1-methyl-urea

This compound shows a more complex solubility behavior due to the presence of a urea functional group and multiple chlorine substitutions.

  • Water Solubility: Likely limited due to the hydrophobic nature of the chlorinated aromatic system and the bulky substituent groups.
  • Organic Solvent Compatibility: More favorable solubility in non-polar to moderately polar solvents, such as dimethyl sulfoxide (DMSO) or chloroform.
  • Complex Interactions: The hydrogen bonding capability of the urea group can enhance solubility to some extent but may not overcome the hydrophobic influences.

In summary, both compounds showcase varied solubility profiles, influenced by their structural features and the nature of the solvents used. Understanding these solubility properties is essential for applications in fields such as pharmaceuticals and environmental chemistry.

Interesting facts

Interesting Facts about 2,4-Dichloro-1-(4-nitrophenoxy)benzene

This compound, also known by its common name, possesses a fascinating blend of properties and applications. Here are some notable facts:

  • Environmental Relevance: 2,4-dichloro-1-(4-nitrophenoxy)benzene is often studied for its role as a contaminant in various ecosystems. Understanding its behavior helps assess environmental health.
  • Biological Activity: This compound exhibits significant biological activity, making it a subject of interest in pharmaceuticals and agrochemicals.
  • Synthesis and Structure: The synthesis of this compound can involve various methods, including halogenation and substitution reactions, leading to a complex structure rich in chlorine and nitro groups.
  • Applications: It finds applications in organic synthesis and as an intermediate in the development of other chemical compounds.

As an example of how chemical modifications can lead to compounds with various functionalities, studying this compound can inspire innovative research in both environmental science and medicinal chemistry.

Interesting Facts about 3-(3,4-Dichlorophenyl)-1-methoxy-1-methyl-urea

This compound is a noteworthy member of the urea class, with unique properties and potential applications in various fields. Here are some fascinating insights:

  • Pest Control: 3-(3,4-dichlorophenyl)-1-methoxy-1-methyl-urea is often explored for its herbicidal properties, particularly in agricultural chemistry.
  • Mechanism of Action: As a urea derivative, it plays a critical role in disrupting the metabolic pathways of target plants, making it effective in controlling unwanted vegetation.
  • Research Applications: Insights gained from studying this compound contribute to the understanding of urea derivatives and their mechanisms, aiding in the design of more efficient agrochemicals.
  • Potential Health Impacts: Investigating this chemical also raises questions regarding its safety and the need for assessment in terms of human and ecological health.

Overall, the significance of this compound in environmental chemistry and agriculture highlights the importance of ongoing research in understanding and optimizing chemical applications.

Synonyms
AGN-PC-0JKHT9
8075-80-7
DTXSID70274776