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Fluometuron

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Identification
Molecular formula
C10H11Cl3FNO
CAS number
2164-17-2
IUPAC name
2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide
State
State

Fluometuron is typically a solid at room temperature.

Melting point (Celsius)
164.50
Melting point (Kelvin)
437.65
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
243.55g/mol
Molar mass
243.5540g/mol
Density
1.5030g/cm3
Appearence

Fluometuron typically appears as a white crystalline solid.

Comment on solubility

Solubility of 2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide

The solubility of 2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide is influenced by its structural components and functional groups. Understanding solubility is crucial for determining the compound's behavior in various environments. Here are some key points to consider:

  • Polarity: The presence of a fluoro group and multiple chloro substituents suggests a degree of polarity, which can enhance solubility in polar solvents like water.
  • Solvent Interactions: This compound may exhibit different solubility properties in organic solvents versus aqueous environments, reflecting its functional groups' compatibility with different solvent types.
  • Hydrogen Bonding: The acetamide functional group can engage in hydrogen bonding, which may facilitate solubility in polar solvents and influence solvent interactions.

As a rule of thumb, the more similar the solvent is to the solute (in terms of polarity), the greater the likelihood of solubility. Thus, it is often summarized that:

"Like dissolves like."

Ultimately, while specific quantitative data on the solubility of 2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide may not be readily available, the theoretical insights can provide a basis for understanding its likely behavior in various chemical contexts.

Interesting facts

Interesting Facts About 2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide

2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide is a compound of significant interest in the field of pharmaceuticals and agricultural chemistry. Here are some compelling insights into its properties and applications:

  • Pharmaceutical Potential: This compound has been studied for its potential therapeutic roles, particularly as an *antimicrobial agent*. Compounds with fluorine substitutions often exhibit enhanced biological activity, making them valuable in drug development.
  • Chlorinated Aromatics: The presence of the trichlorophenyl group makes this compound a unique example of chlorinated aromatics, which are known for their *biological activity* and utility in various chemical processes.
  • Substituent Effects: The fluorine atom in the 2-position can significantly influence the compound's overall reactivity and stability. This can lead to altered interactions with biological systems, making it a subject of interest for *research in medicinal chemistry*.
  • Environmental Considerations: Compounds containing trichlorophenyl moieties are often scrutinized for their ecological impact. Understanding the degradation pathways and behavior of such compounds in the environment is crucial for assessing their *sustainability* and safety.
  • Structure-Activity Relationship (SAR): The exploration of structure-activity relationships is essential in medicinal chemistry. Researchers often modify the chemical structure of such compounds to elucidate *key interactions* that lead to increased efficacy or reduced toxicity in biological systems.

In summary, 2-fluoro-N-methyl-N-(2,4,5-trichlorophenyl)acetamide serves as an intriguing case study in the integration of fluorinated and chlorinated compounds in chemical research. Its unique structural features offer opportunities for innovation in drug design and environmental chemistry.

Synonyms
10015-99-3
BRN 2127532
2-Fluoro-N-methyl-2',4',5'-trichloroacetanilide
ACETANILIDE, 2-FLUORO-N-METHYL-2',4',5'-TRICHLORO-
DTXSID10142980
DTXCID1065471