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2-Chloro-1-(2,4-dichlorophenyl)ethanone

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Identification
Molecular formula
C8H5Cl3O
CAS number
20298-86-6
IUPAC name
2-chloro-1-(2,4-dichlorophenyl)ethanone
State
State
At room temperature, 2-Chloro-1-(2,4-dichlorophenyl)ethanone exists as a solid. It may also appear as slightly oily when impurities are present or when it is described as not entirely pure, allowing for partial liquefaction.
Melting point (Celsius)
43.00
Melting point (Kelvin)
316.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
209.46g/mol
Molar mass
209.4560g/mol
Density
1.4299g/cm3
Appearence
2-Chloro-1-(2,4-dichlorophenyl)ethanone is described as a colorless to pale yellow crystalline solid. It is known to be moisture-sensitive, and exposure to air can lead to its slow decomposition, resulting in a darker appearance.
Comment on solubility

Solubility of 2-chloro-1-(2,4-dichlorophenyl)ethanone

2-chloro-1-(2,4-dichlorophenyl)ethanone, with its complex structure, exhibits interesting solubility characteristics that are essential for its applications in various fields. Generally, the solubility of this compound can be influenced by several factors, including:

  • Polarity: The presence of chlorine atoms in its molecular structure contributes to a degree of polarity that can affect solubility in polar solvents.
  • Temperature: As with many organic compounds, increasing temperature may enhance solubility, making it more effective in certain conditions.
  • Solvent Nature: This compound is expected to be more soluble in organic solvents (e.g., ethanol, acetone) compared to water due to its organic nature.

While the precise solubility in various solvents can vary, it is typically seen that:

  • Alcohols: Often enhance solubility due to similar functional groups.
  • Aromatics: Can solubilize due to π-π interactions with the chlorinated phenyl groups.
  • Water: May not be a suitable solvent due to the compound's hydrophobic characteristics.

In summary, the solubility of 2-chloro-1-(2,4-dichlorophenyl)ethanone illustrates the intricate relationship between molecular structure and solvent interaction, emphasizing the importance of selecting the right solvent for effective utilization in chemical processes.

Interesting facts

Interesting Facts about 2-Chloro-1-(2,4-dichlorophenyl)ethanone

2-Chloro-1-(2,4-dichlorophenyl)ethanone, also known as a significant chemical intermediate in the synthesis of various organic compounds, showcases fascinating properties and applications.

Key Insights:

  • Versatile Building Block: It is often utilized in the synthesis of pharmaceuticals and agrochemicals, highlighting its importance in the creation of effective medicinal and agricultural products.
  • Structure Significance: The presence of multiple chlorine atoms in its structure contributes to its reactivity and ability to participate in various chemical reactions such as Friedel-Crafts acylation.
  • Chlorinated Compounds: Compounds like this one play a crucial role in medicinal chemistry due to their enhanced biological activity compared to their non-chlorinated counterparts.
  • Environmental Considerations: Due to the presence of chlorine, it is essential to study and manage the environmental impact of this compound, particularly its potential accumulation and persistence in ecosystems.
  • Safety Matter: As with many chlorinated compounds, handling 2-chloro-1-(2,4-dichlorophenyl)ethanone requires caution due to potential toxicity and the need for appropriate safety protocols.

In the realm of chemistry, compounds like 2-chloro-1-(2,4-dichlorophenyl)ethanone remind us of how intricate and interconnected chemical synthesis can be. It serves as a testament to the importance of understanding chemical structures, their reactivity, and the potential benefits and risks they may pose in real-world applications. Indeed, as the renowned chemist Linus Pauling once said, "The best way to have a good idea is to have lots of ideas." In that spirit, exploring this compound can enrich our understanding and inspire future innovations in chemical sciences.

Synonyms
2,2',4'-Trichloroacetophenone
2-Chloro-1-(2,4-dichlorophenyl)ethanone
2,4-Dichlorophenacyl chloride
CCRIS 633
EINECS 224-218-2
UNII-2E35P7HJI2
2E35P7HJI2
DTXSID3026190
DTXCID506190
EC 224-218-2
2,4,.omega.-Trichloroacetophenone
Acetophenone, 2,2',4'-trichloro-
omega-Chloro-2,4-dichloroacetophenone
.omega.-Chloro-2,4-dichloroacetophenone
TRICHLOROACETOPHENONE, 2,2',4'-
2,2',4'Trichloroacetophenone
2,4,omega-Trichloroacetophenone
alpha-2,4-Trichloroacetophenone
alpha,2',4'Trichloroacetophenone
omegaChloro2',4'dichloroacetophenone
2Chloro1(2,4dichlorophenyl)ethanone
2,4,2'-TRICHLOROACETOPHENONE
2-CHLORO-1-(2',4'-DICHLOROPHENYL)ETHANONE
un1759
vywpprljnvhpeu-uhfffaoysa-n
4252-78-2
2-chloro-1-(2,4-dichlorophenyl)ethan-1-one
Ethanone, 2-chloro-1-(2,4-dichlorophenyl)-
alpha,2,4-Trichloroacetophenone
.alpha.,2,4-Trichloroacetophenone
Chloromethyl 2,4-dichlorophenyl ketone
NCGC00091258-01
NCGC00091258-02
CAS-4252-78-2
MFCD00000934
2,2',4'-TRICHLORO PHENYL ETHANONE
1-(2,4-dichlorophenyl)-2-chloroethan-1-one
?,2,4-Trichloroacetophenone
2,4-Dichlorphenacyl chloride
SCHEMBL1691536
2,2`,4`-Trichloroacetophenone
CHEMBL1569226
2,2', 4'-trichloroacetophenone
2,4-Dichloro-a-chloroacetophenone
2, 2', 4'-trichloroacetophenone
2,2\',4\'-Trichloroacetophenone
BCP17104
STR01461
Tox21_113246
Tox21_113461
Tox21_200671
STK498199
AKOS000118912
Tox21_113461_1
2,2',4'-Trichloroacetophenone, 97%
2-chloro-1-(2,4dichlorophenyl)ethanone
NCGC00091258-03
NCGC00091258-04
NCGC00091258-05
NCGC00258225-01
AC-10643
PD014808
2-chloro-1-(2,4-dichlorophenyl)-ethanone
DB-019589
2-chloranyl-1-(2,4-dichlorophenyl)ethanone
CS-0008216
NS00002202
T1405
EN300-17947
1-(2,4-dichlorophenyl)-2-chloroethan-1 -one
2-chloro-1-(2', 4'-dichlorophenyl) ethanon
2-chloro-1-(2,4-dichlorophenyl)-ethan-1-one
E80406
A825923
Q10844265
Z57127890
F0001-1181
2,2 inverted exclamation marka,4 inverted exclamation marka-Trichloroacetophenone