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Clomazone

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Identification
Molecular formula
C11H13ClN2O2
CAS number
81777-89-1
IUPAC name
1-(3-chloro-4-methoxy-phenyl)-3-methyl-urea
State
State

At room temperature, Clomazone is in a solid, crystalline state. It is stable under normal conditions and used primarily in this form for its intended applications.

Melting point (Celsius)
59.00
Melting point (Kelvin)
332.15
Boiling point (Celsius)
535.90
Boiling point (Kelvin)
809.05
General information
Molecular weight
238.69g/mol
Molar mass
238.6800g/mol
Density
1.3970g/cm3
Appearence

Clomazone appears as a white to off-white crystalline powder. It is typically odorless and often used in its solid form for agricultural applications.

Comment on solubility

Solubility of 1-(3-chloro-4-methoxy-phenyl)-3-methyl-urea

The solubility of 1-(3-chloro-4-methoxy-phenyl)-3-methyl-urea can be particularly intriguing due to its chemical structure and functional groups. This compound, featuring a urea moiety with aromatic substituents, exhibits solubility characteristics that are influenced by both hydrophilic and hydrophobic interactions.

Key Points on Solubility:

  • Polar Nature: The presence of the urea group contributes to the polar character of the compound, enhancing its solubility in polar solvents.
  • Aromatic Interactions: The chloro and methoxy groups located on the phenyl ring may impact solubility in non-polar solvents, possibly leading to reduced solubility.
  • Solvent Dependency: This compound is generally more soluble in organic solvents such as ethanol or dimethyl sulfoxide (DMSO) when compared to water.

It is essential to note that solubility can vary based on factors such as temperature, pH, and the specific solvent used. Consequently, conducting comprehensive solubility tests would provide a better understanding of its behavior in various environments.

In summary, while 1-(3-chloro-4-methoxy-phenyl)-3-methyl-urea displays reasonable solubility in polar solvents, its application in non-polar environments requires careful consideration of the solvation dynamics involved.

Interesting facts

Interesting Facts about 1-(3-Chloro-4-methoxy-phenyl)-3-methyl-urea

1-(3-Chloro-4-methoxy-phenyl)-3-methyl-urea is a noteworthy compound in the realm of organic chemistry, particularly due to its diverse applications and interesting structural features. This compound can be explored from several angles:

  • Biological Significance: Many derivatives of urea, including this compound, have shown potential in pharmaceutical development. Studies indicate that compounds with similar structures may exhibit antitumor and antimicrobial properties, making them a subject of interest for drug discovery.
  • Targeted Modifications: The presence of the chloro and methoxy groups in its structure allows for interesting variations in reactivity. This opens doors for chemists to experiment with the compound and develop new derivatives through substitution reactions.
  • Structural Intricacy: The ability of 1-(3-Chloro-4-methoxy-phenyl)-3-methyl-urea to form hydrogen bonds due to the urea functional group contributes to its potential stability and reactivity in various chemical environments.
  • Environmental Aspect: Research on similar compounds often emphasizes the importance of studying their environmental impact, particularly if they are being investigated for agricultural uses, such as herbicides or pesticides.

In medicinal chemistry, the study of derivatives like 1-(3-chloro-4-methoxy-phenyl)-3-methyl-urea can provide insights into designing more effective therapies. As the field of chemistry continues to evolve, the potential applications of such compounds will undoubtedly expand, enhancing our understanding of their role in both health and the environment.

Synonyms
20782-57-4
Urea, N-(3-chloro-4-methoxyphenyl)-N'-methyl-
1-(3-chloro-4-methoxyphenyl)-3-methylurea
3-(3-chloro-4-methoxylphenyl)-1-methylurea
Metoxuron-monomethyl
metoxuron-monodemethyl
Metoxuron-monomethyl 10 microg/mL in Ethyl acetate
SCHEMBL11754054
DTXSID20174873
CHEBI:157702
YWHRNWZTCCNWSH-UHFFFAOYSA-N
N'-(3-chloro-4-methoxylphenyl)-N-methylurea
N-methyl-N'-(3-chloro-4-methoxyphenyl)-urea