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2',4'-Dichloroacetophenone

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Identification
Molecular formula
C8H6Cl2O
CAS number
2234-16-4
IUPAC name
1-(2,4-dichlorophenyl)ethanone
State
State

The compound is in a solid state at room temperature, commonly found in crystalline form with a tendency to sublimate slowly on prolonged exposure to air.

Melting point (Celsius)
41.50
Melting point (Kelvin)
314.65
Boiling point (Celsius)
246.00
Boiling point (Kelvin)
519.15
General information
Molecular weight
175.03g/mol
Molar mass
175.0360g/mol
Density
1.3550g/cm3
Appearence

2',4'-Dichloroacetophenone typically appears as an off-white to pale yellow crystalline solid. The crystals may exhibit a slightly greasy texture. It has a distinctive, pungent odor.

Comment on solubility

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

The solubility of 1-(2,4-dichlorophenyl)ethanone, a compound that falls under the category of ketones, can be characterized as follows:

  • Solvent Compatibility: This compound exhibits moderate solubility in organic solvents such as ethanol, acetone, and chloroform, but is typically insoluble or has limited solubility in water.
  • Polarity Considerations: The presence of the dichlorophenyl group contributes to the overall polarity of the molecule, making it more soluble in polar organic solvents compared to non-polar solvents.
  • Temperature Effects: Like many organic compounds, the solubility of 1-(2,4-dichlorophenyl)ethanone can increase with temperature; thus, higher temperatures might enhance its dissolution in suitable solvents.
  • Practical Applications: This solubility profile is particularly important in various chemical processes, including synthesis and extraction techniques, where the choice of solvent impacts the efficiency of the reaction.

In summary, while 1-(2,4-dichlorophenyl)ethanone is not highly soluble in water, its decent solubility in polar organic solvents offers useful avenues for its application in laboratory settings.

Interesting facts

Interesting Facts about 1-(2,4-Dichlorophenyl)ethanone

1-(2,4-Dichlorophenyl)ethanone is a fascinating compound that demonstrates the unique interplay of functional groups and aromatic chemistry. It is primarily utilized in the field of organic synthesis and can serve as an important precursor in the production of various pharmaceuticals and agrochemicals. Here are some noteworthy aspects of this compound:

  • Aromatic Structure: With a dichlorophenyl group, this compound exhibits enhanced stability and reactivity due to the presence of chlorine substituents, which can influence both electron density and resonance in the aromatic ring.
  • Role in Synthesis: It is commonly employed as a building block in organic synthesis, particularly in the creation of complex molecules. As a ketone, it possesses a reactive carbonyl group that can undergo various chemical reactions such as nucleophilic additions.
  • Applications: The compound finds its place in the synthesis of pharmaceuticals, including analgesics and anti-inflammatory agents, showcasing its significance in medicinal chemistry.
  • Environmental Consideration: The presence of chlorine in its structure raises concerns regarding environmental impact and toxicity. Care must be taken during its synthesis and disposal, emphasizing the importance of green chemistry approaches.
  • Research Insights: Studies on the reactivity of 1-(2,4-dichlorophenyl)ethanone often reveal insights into reaction mechanisms, offering a platform for understanding the behavior of similar carbonyl compounds.

As you delve into the world of this compound, remember that its chemical properties are intertwined with practical applications that influence both industry and research. The world of chemistry is indeed a dynamic field, and 1-(2,4-dichlorophenyl)ethanone stands as a testament to the complexities and innovations that it encompasses.

Synonyms
2',4'-Dichloroacetophenone
2234-16-4
1-(2,4-Dichlorophenyl)ethanone
2,4-Dichloroacetophenone
Ethanone, 1-(2,4-dichlorophenyl)-
1-(2,4-Dichlorophenyl)ethan-1-one
Acetophenone, 2',4'-dichloro-
p-Chloro-2-chloroacetophenone
EINECS 218-780-8
NSC 33945
UNII-T7F2608H5H
o,p-dichloroacetophenone
T7F2608H5H
NSC-33945
DTXSID1022182
EC 218-780-8
2-ACETYL-5-CHLOROPHENYL CHLORIDE
DTXCID602182
Acetophenone, 2',4'-dichloro-(8CI)
inchi=1/c8h6cl2o/c1-5(11)7-3-2-6(9)4-8(7)10/h2-4h,1h
xmcrwebercxjch-uhfffaoysa-n
MFCD00000581
2,4-dichoroacetophenone
1-(2,4-Dichlorophenyl)ethanone; 2-Acetyl-5-chlorophenyl Chloride; NSC 33945; o,p-Dichloroacetophenone; p-Chloro-2-chloroacetophenone
2`,4`-Dichloroacetophenone
(2,4-dichlorophenyl)ethanone
SCHEMBL322161
2',4'-Dichloroacetophenone, 96%
NSC33945
STR06706
1-(2,4-Dichlorophenyl)ethanone #
BBL027300
STK397561
AKOS000119380
AC-2996
CS-W015972
FD45894
PS-3392
SY003527
DB-030786
A4797
D1490
NS00001049
EN300-20238
S12308
Q2813775
F0850-6804
Z104477446
2 inverted exclamation mark ,4 inverted exclamation mark -Dichloroacetophenone