Interesting facts
Interesting Facts About Ethyl 10-(4-Iodophenyl)undecanoate
Ethyl 10-(4-iodophenyl)undecanoate is a fascinating compound that belongs to the category of long-chain fatty acid esters. Its unique structural components yield a variety of interesting properties and potential applications.
Key Features
- Biological Significance: Due to the presence of the 4-iodophenyl group, this compound may exhibit interesting biological activities, making it a candidate for pharmaceutical research.
- Utility in Organic Synthesis: As an ester, it can participate in various organic reactions, including transesterification and hydrolysis, thus serving as an essential building block in synthetic chemistry.
- Hydrophobic Characteristics: The long undecanoate chain provides a hydrocarbon portion that can influence the solubility and interaction of the compound in lipid environments, making it of interest in studies related to membrane biochemistry.
Potential Applications
- Drug Development: The intriguing combination of elements in its structure could be explored for the development of new pharmaceuticals.
- Material Science: As a fatty ester, it could find applications in creating novel materials with unique properties.
- Nanotechnology: Its characteristics may be exploited in the creation of nanoparticles or as a component in drug delivery systems.
As with many synthetic compounds, further studies may reveal more of its secrets. Scientists are continuously exploring the *versatility* of ethyl 10-(4-iodophenyl)undecanoate, and it may unlock potential in both academic and industrial realms.
In the world of chemistry, compounds such as this spark *curiosity* and lead to exciting advancements, emphasizing the importance of continued research and discovery.
Synonyms
Iofendylate
ethyl 10-(4-iodophenyl)undecanoate
99-79-6
Iofendilato
Iofendylatum
Ethiodan
Ethyl 10-(p-iodophenyl)undecylate
Ethyl 10-(p-iodophenyl)hendecanoate
6V3I57K9UL
Jofendylatum
Iophendylate, p-
Mulsopaque
Neurotrast
Myodil
Myodyl
Mulsopaque; Myodil; Myodyl; Neurotrast; Pantopaque
Iofendylatum [INN-Latin]
Iofendilato [INN-Spanish]
HSDB 3346
Ethyl 10-(p-iodophenyl)undecanoate
Iofendylate [INN:BAN]
EINECS 202-787-8
BRN 2661373
UNII-6V3I57K9UL
p-Iophendylate
Undecanoic acid, 10-(p-iodophenyl)-, ethyl ester
JOFENDYLATE
Benzenedecanoic acid, 4-iodo-iota-methyl-, ethyl ester
IOPHENDYLATE [MI]
CHEMBL951
3-09-00-02627 (Beilstein Handbook Reference)
SCHEMBL492663
DTXSID2052869
LAYLQVBQIBQVLL-UHFFFAOYSA-N
ethyl10-(4-iodophenyl)undecanoate
HY-A0223
AKOS005267217
DA-54356
CS-0017569
NS00040560
Q3801357
BENZENEDECANOIC ACID, 4-IODO-.IOTA.-METHYL-, ETHYL ESTER
Solubility of Ethyl 10-(4-iodophenyl)undecanoate
Ethyl 10-(4-iodophenyl)undecanoate, a compound with the formula C19H29IO, exhibits unique solubility characteristics that can be influenced by several factors. Here are some key points to consider regarding its solubility:
In summary, while ethyl 10-(4-iodophenyl)undecanoate shows favorable solubility in organic solvents, its poor solubility in water highlights the hydrophobic nature imparted by its long carbon chain. Understanding these solubility traits is crucial for applications involving this compound.