Interesting facts
Interesting Facts about 1,2-bis(4-chlorophenyl)ethane-1,2-dione
1,2-bis(4-chlorophenyl)ethane-1,2-dione, commonly referred to in scientific literature as a potent organic compound, carries significant relevance in the field of organic chemistry and pharmaceutical sciences. Here are some intriguing aspects of this compound:
- Structural Composition: This compound features a unique structure where two 4-chlorophenyl groups are attached to a central ethane-1,2-dione. The arrangement provides distinct electronic properties that contribute to its reactivity.
- Medicinal Applications: Due to its functional groups, the compound is investigated for its potential biological activity. It has been studied for possible applications in developing pharmaceuticals, particularly as a precursor for synthesizing other biologically active molecules.
- Role in Synthesis: As an intermediate compound, it serves as a valuable building block in organic synthesis. Its versatile nature allows chemists to create diverse derivatives through further reactions, making it a favorite in the laboratory.
- Significance in Research: The study of 1,2-bis(4-chlorophenyl)ethane-1,2-dione has led to insights into reaction mechanisms and the development of new synthetic methodologies, contributing to advancements in organic chemistry.
- Environmental Considerations: Chloro-substituted compounds, while useful, also raise concerns regarding environmental impact. Understanding their chemical behavior helps chemists design better waste management strategies and reduce potential toxicity.
In conclusion, 1,2-bis(4-chlorophenyl)ethane-1,2-dione is more than just a compound; it embodies a bridge between theoretical chemistry and practical applications in medicine and synthesis. As a science student or researcher, delving into the properties and applications of this compound can unveil exciting opportunities for discovery and innovation.
Synonyms
4,4'-Dichlorobenzil
3457-46-3
BIS(4-CHLOROPHENYL)ETHANEDIONE
4,4'-Dichlorodibenzoyl
Ethanedione, bis(4-chlorophenyl)-
Bis(p-chlorophenyl)ethanedione
Benzil, 4,4'-dichloro-
NSC 274
EINECS 222-387-7
AI3-15871
DTXSID4063038
1,2-Ethanedione, 1,2-bis(4-chlorophenyl)-
DTXCID1038874
222-387-7
1,2-bis(4-chlorophenyl)ethane-1,2-dione
1,2-Bis-(4-chloro-phenyl)-ethane-1,2-dione
88372-92-3
bis(4-chlorophenyl)ethane-1,2-dione
MFCD00018685
1,2-bis(4-chlorophenyl)-1,2-ethanedione
4,4//'-Dichlorobenzil
dichlorbenzil
NSC274
p-p'-Dichloro-benzil
Benzil,4'-dichloro-
4,4'-Dichlorobibenzoyl
Benzil-based compound, 9
SCHEMBL273857
CHEMBL192139
BDBM22731
NSC-274
HMS3740A17
CS-M0252
STK537320
AKOS001053129
PD119753
SY017129
TS-00966
DB-048652
D4440
NS00029686
EN300-04843
F11776
1,2-BIS(4-CHLOROPHENYL)ETHAN-1,2-DIONE
AQ-917/40154799
Z56922048
Ethanedione,bis(4-chlorophenyl)-,radical ion(1-)(9ci)
F3096-2307
Bis(p-chlorophenyl)ethanedione;1,2 - bis(4 - chlorophenyl)ethane - 1,2 - dione
Solubility of 1,2-bis(4-chlorophenyl)ethane-1,2-dione
The solubility of 1,2-bis(4-chlorophenyl)ethane-1,2-dione, a complex aromatic compound, can be described as follows:
In conclusion, the solubility behavior of 1,2-bis(4-chlorophenyl)ethane-1,2-dione illustrates a classic case of aromatic compounds, where polarity and solvent choice play crucial roles. Understanding these factors is essential for effective application in chemical processes.