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
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:
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.