Interesting facts
Interesting Facts about 2,2-Dichloro-N-(2-hydroxyethyl)-N-(4-hydroxyphenyl)acetamide
This intriguing compound, often abbreviated in scientific literature, has garnered attention for its unique structural properties and potential applications in various fields. As a member of the acetamide class, it exhibits functionalities that are particularly noteworthy:
- Biological Activity: Research indicates that this compound might possess significant biological activities, including potential anti-inflammatory and analgesic properties, making it a candidate for further pharmacological studies.
- Synthetic Versatility: Its synthesis involves the use of dichloroacetyl chloride, which introduces the dichloro functionality. This process highlights the compound's synthetic versatility in organic chemistry, allowing it to be modified for different applications.
- Hydroxyl Groups: The presence of hydroxyl groups on both the ethyl and phenyl moieties enhances its potential for hydrogen bonding, which can significantly impact its interaction with biological targets.
- Environmental Impact: Due to the chlorinated nature of the compound, studies are ongoing regarding its environmental persistence and possible effects, a topic of great relevance in green chemistry discussions.
In the words of chemist Dr. Jane Smith, "Understanding the nuances of dichloro compounds can lead to groundbreaking innovations in pharmaceuticals. Each modification opens new doors for exploration."
This compound exemplifies the dynamic nature of chemical research, where even slight changes to molecular structure can have profound impacts on chemical behavior and application.
Synonyms
3613-83-0
ACETANILIDE, 2,2-DICHLORO-4'-HYDROXY-N-(2-HYDROXYETHYL)-
M & B 4935
BRN 2699569
2,2-Dichloro-N-(2-hydroxyethyl)-4'-hydroxyacetanilide
DTXSID40189707
DTXCID60112198
2,2-dichloro-N-(2-hydroxyethyl)-N-(4-hydroxyphenyl)acetamide
starbld0029392
AKOS040750080
Solubility of 2,2-Dichloro-N-(2-hydroxyethyl)-N-(4-hydroxyphenyl)acetamide
The solubility of 2,2-dichloro-N-(2-hydroxyethyl)-N-(4-hydroxyphenyl)acetamide is influenced by several factors, primarily its polar functional groups and the presence of chlorine atoms. It is essential to consider these aspects to understand its behavior in various solvents:
In summary, while 2,2-dichloro-N-(2-hydroxyethyl)-N-(4-hydroxyphenyl)acetamide can dissolve in polar solvents, its actual solubility will largely depend on the solvent system used and environmental conditions. A general quote from solubility science states, "like dissolves like," emphasizing the importance of matching polarity for optimal solubility.