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Fluometuron

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Identification
Molecular formula
C10H10Cl2F3NO
CAS number
2164-17-2
IUPAC name
1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea
State
State

The compound is solid at room temperature, remaining stable under normal conditions without undergoing any phase change.

Melting point (Celsius)
164.00
Melting point (Kelvin)
437.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
332.69g/mol
Molar mass
332.6910g/mol
Density
1.5630g/cm3
Appearence

Fluometuron appears as a white crystalline solid. The crystals are typically small and may appear powdery to granular. When observed in mass or under a microscope, the structure may seem opaque to slightly translucent.

Comment on solubility

Solubility of 1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea

The solubility of 1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea can be complex and is influenced by various factors. Here are some key points to consider:

  • Polarity: This compound contains both chlorinated aromatic groups and a urea functional group, which can lead to increased polarity. This increased polarity often enhances the solubility in polar solvents.
  • Solvent Choice: In general, compounds with similar polarities tend to dissolve well in each other. Therefore, this urea derivative may exhibit notable solubility in solvents such as water, methanol, or DMSO (dimethyl sulfoxide), while being less soluble in non-polar solvents.
  • Temperature Effects: The solubility could also vary with temperature; higher temperatures may increase solubility through enhanced molecular motion.
  • pH Influence: The pH of the solution might play a role due to the nature of the urea group, potentially affecting its protonation state and overall solubility.

Due to these factors, it is crucial to conduct empirical studies to determine the exact solubility in various solvents under different conditions." Look for the phrase: "like dissolves like." This adage is a guiding principle in predicting solubility behavior.

In conclusion, while we can hypothesize the solubility characteristics of 1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea, definitive solubility values must be determined through experimental procedures to fully understand its behavior in specific environments.

Interesting facts

Exploring 1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea

1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea is a compound that has gained significance in various scientific fields, particularly in medicinal chemistry and agricultural applications. Here are some intriguing facts about this compound:

  • Pharmaceutical Relevance: This compound is known for its role in the development of pharmaceuticals, particularly as a potential candidate for targeting specific biological pathways.
  • Pest Control: Due to its structural characteristics, it has been investigated for its effectiveness as a pesticide, contributing to higher crop yields and pest management solutions.
  • Fluorine Atoms: The presence of trifluoromethyl groups enhances the compound's metabolic stability and lipophilicity, making it an interesting subject of study in drug design.
  • Structural Hybrids: The dual chlorination offers exciting avenues for creating hybrid molecules that may exhibit enhanced biological activity.

As a scientist or a student delving into the complexities of chemical compounds, it's fascinating to consider how subtle changes in molecular structure can lead to significant differences in a compound's properties and applications. "Understanding the relationship between structure and function is fundamental in the field of chemistry." This notion rings true with 1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea, exemplifying how chemistry merges with real-world applications to address challenges in health and agriculture.

Synonyms
Halocarban
Cloflucarban
369-77-7
Cloflucarbon
Irgasan CF3
Halocarbano
Halocarbanum
Trifluoromethyldichlorocarbanilide
Cloflucarban [USAN]
Halocarban [INN]
4,4'-Dichloro-3-(trifluoromethyl)carbanilide
UNII-I5ZZY3DC5G
I5ZZY3DC5G
Halocarbanum [INN-Latin]
Halocarbano [INN-Spanish]
Halocarban (INN)
NSC-114133
1-(4-chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea
Cloflucarban (USAN)
DTXSID0048684
1-[4-CHLORO-3-(TRIFLUOROMETHYL)PHENYL]-3-(4-CHLOROPHENYL)UREA
EINECS 206-724-5
CLOFLUCARBAN [MI]
NSC114133
NSC 114133
HALOCARBAN [WHO-DD]
DTXCID0028610
CHEBI:135477
Urea, N-(4-chlorophenyl)-N'-(4-chloro-3-(trifluoromethyl)phenyl)-
3-Trifluoromethyl-4,4'-dichloro-N,N'-diphenylurea
Carbanilide, 4,4'-dichloro-3-(trifluoromethyl)- (8CI)
TFC
1-(4-Chlorphenyl)-3-(4-chlor-3-trifluormethylphenyl)urea
NCGC00185743-01
N-(4-Chlorophenyl)-N'-(4-chloro-3-(tifluoromethyl)phenyl)urea
Urea, N-(4-chlorophenyl)-N'-[4-chloro-3-(trifluoromethyl)phenyl]-
Halocarbanum (INN-Latin)
4,4'-Dichloro-3-(trifluoromethyl)-carbanilide
Halocarbano (INN-Spanish)
Carbanilide, 4,4'-dichloro-3-(trifluoromethyl)-
N-(4-Chlorophenyl)-N'-(4-chloro-3-(trifluoromethyl)phenyl)urea
CAS-369-77-7
3-Trifluoromethyl-4,4'-dichlorocarbanilide
N-(4-chlorophenyl)-N'-[4-chloro-3-(trifluoromethyl)phenyl]urea
Cloflucarban(USAN)
MFCD00867294
CLOFLUCARBAN [INCI]
MLS004774004
SCHEMBL119821
CHEMBL1981438
Tox21_113070
3-Trifluoromethyl-4,N'-diphenylurea
AKOS001047813
Tox21_113070_1
NCGC00185743-02
AS-56259
DA-62401
SMR001798711
HY-116587
CS-0065987
NS00013539
3-(Trifluoromethyl)-4,4'-dichlorocarbanilide
Carbanilide,4'-dichloro-3-(trifluoromethyl)-
D03548
EN300-342755
G76701
BRD-K31002570-001-01-2
Q27280484
Z44608704
Carbanilide, 4,4'-dichloro-3-(trifluoromethyl)-(8CI)
3-[4-chloro-3-(trifluoromethyl)phenyl]-1-(4-chlorophenyl)urea
1-(4-Chlorophenyl)-3-[4-chloro-3-(trifluoromethyl)phenyl]urea, 97%