Interesting facts
Exploring 1-(2,3,4-trichlorophenyl)ethanone
1-(2,3,4-trichlorophenyl)ethanone, a compound with intriguing properties and applications, is noteworthy within the realm of organic chemistry. This molecule is characterized by its unique structure, featuring a trichlorophenyl group attached to an ethanone moiety. Here are some fascinating facts about this compound:
- Structural Significance: The presence of three chlorine atoms on the phenyl ring introduces significant electron-withdrawing effects, which can enhance the compound's reactivity in various chemical reactions.
- Synthesis and Applications: 1-(2,3,4-trichlorophenyl)ethanone can be synthesized through effective organic reactions, often serving as an intermediate in the path of pharmaceuticals or agrochemicals. Its synthetic versatility makes it a valuable building block in organic synthesis.
- Toxicological Concerns: Due to the chlorinated nature of this compound, it’s essential to handle it with caution. The chlorine substituents may contribute to toxicity, which necessitates safety protocols during laboratory handling.
- Reactivity: The ketone functional group present in the compound allows for various chemical reactions such as nucleophilic addition, making it an interesting subject for study in reaction mechanisms.
- Research Potential: Ongoing research into chlorinated compounds like this one focuses on their environmental impact and biological effects, underscoring the necessity for understanding such chemicals in current scientific discourse.
The study of 1-(2,3,4-trichlorophenyl)ethanone exemplifies the interplay between structure and reactivity in organic chemistry. As scientists continue to explore its potential applications and implications, this compound remains a compelling topic for both research and education.
Synonyms
2',3',4'-TRICHLOROACETOPHENONE
1-(2,3,4-Trichlorophenyl)ethanone
2,3,4-Trichloroacetophenone
CCRIS 785
EINECS 237-092-9
UNII-8HVD33N785
DTXSID2022256
8HVD33N785
DTXCID502256
BXJZZJYNVIDEKG-UHFFFAOYSA-
TRICHLOROACETOPHENONE, 2',3',4'-
2',3',4'Trichloroacetophenone
BXJZZJYNVIDEKG-UHFFFAOYSA-N
InChI=1/C8H5Cl3O/c1-4(12)5-2-3-6(9)8(11)7(5)10/h2-3H,1H3
UN1759
13608-87-2
Ethanone, 1-(2,3,4-trichlorophenyl)-
1-(2,3,4-trichlorophenyl)ethan-1-one
Acetophenone, 2',3',4'-trichloro-
MFCD00000542
1-acetyl-2,3,4-trichlorobenzene
MLS002415678
SCHEMBL403103
SCHEMBL1679916
CHEMBL1870723
SCHEMBL30610932
HMS3039P10
2',3',4'-trichloro acetophenone
2',3',4'-trichloro-acetophenone
NAA60887
Tox21_200293
BBL011536
SBB058348
STL146655
AKOS000120305
1-(2,3,4-Trichlorophenyl)ethanone #
2',3',4'-Trichloroacetophenone, 95%
NCGC00091193-01
NCGC00091193-02
NCGC00257847-01
AS-61378
SMR001370873
CAS-13608-87-2
DB-001199
NS00024407
ST50308555
T2306
EN300-20707
D92595
Q27270548
Z104480064
Solubility of 1-(2,3,4-trichlorophenyl)ethanone
The solubility of 1-(2,3,4-trichlorophenyl)ethanone, also known as trichlorophenyl ethanone, exhibits noteworthy characteristics due to its chemical structure. Here are some key points regarding its solubility:
In summary, while 1-(2,3,4-trichlorophenyl)ethanone shows varying solubility depending on the solvent, understanding its interactions with polar and non-polar environments is crucial for effective application in chemical processes. Always consider the solvent's polarity, temperature, and structural characteristics for optimal results.