Interesting facts
Interesting Facts About N-(4-Iodophenyl)acetamide
N-(4-iodophenyl)acetamide is a fascinating compound that plays a significant role in both academic research and practical applications, especially in the fields of medicinal chemistry and organic synthesis. Here are some key points to consider:
- Structure and Functional Groups: This compound features an acetamide functional group, which is a derivative of acetic acid. The presence of the iodine atom on the phenyl ring significantly alters its chemical reactivity and biological activity.
- Biological Activity: Compounds like N-(4-iodophenyl)acetamide are often explored for their potential pharmaceutical properties. They can exhibit various biological activities, including anti-inflammatory and antimicrobial effects, which makes them of interest in drug development.
- Importance in Organic Synthesis: N-(4-iodophenyl)acetamide can be utilized as an intermediate in the synthesis of other complex molecules. The iodine substituent serves as a site for nucleophilic substitution reactions, enabling further chemical transformations.
- Applications in Material Science: Beyond its medicinal properties, this compound may also find utility in material science, particularly in the development of new materials with specific electronic or optical properties.
- Research Potential: Ongoing research into compounds with similar structures often reveals new insights into reaction mechanisms and molecular interactions, which can lead to the discovery of novel therapeutic agents.
In summary, N-(4-iodophenyl)acetamide serves as a prime example of how modifications to simple organic structures can yield diverse and impactful chemical properties. As the field of chemistry continues to evolve, the importance of such compounds in both research and industry cannot be understated.
Synonyms
N-(4-Iodophenyl)acetamide
622-50-4
4-Iodoacetanilide
4'-Iodoacetanilide
p-Iodoacetanilide
Acetamide, N-(4-iodophenyl)-
ACETANILIDE, 4'-IODO-
NSC 2161
BRN 2085726
AI3-23888
DTXSID7060752
4-12-00-01546 (Beilstein Handbook Reference)
para-iodoacetanilide
DTXCID5043267
612-973-4
MFCD00016352
4'-Iodo-acetanilide
Maybridge1_006480
para-acetamino-iodo-benzene
WLN: IR DMV1
N-(4-iodophenyl) acetamide
N-(4-iodophenyl)-acetamide
4-(N-acetylamino)iodobenzene
N-(4-iodo-phenyl)-acetamide
SCHEMBL669782
HMS559O12
Acetamide, N-(4-iodophenyl-)-
NSC2161
NSC-2161
CCG-56184
AKOS002813447
CS-W004143
FI70546
AC-22934
SY051203
I0846
NS00034979
10.14272/SIULLDWIXYYVCU-UHFFFAOYSA-N
EN300-384681
F21272
1Y-0922
AH-034/05420003
doi:10.14272/SIULLDWIXYYVCU-UHFFFAOYSA-N
SR-01000645158-1
Z30316374
Solubility of N-(4-iodophenyl)acetamide
N-(4-iodophenyl)acetamide, with the chemical formula C9H10INO, presents interesting characteristics in terms of its solubility. This compound is a derivative of acetamide featuring an iodine substituent, which influences its interactions with solvents.
When discussing the solubility of N-(4-iodophenyl)acetamide, consider the following points:
In conclusion, while N-(4-iodophenyl)acetamide has specific solubility traits related to its structure, empirical testing is the best way to determine its solubility in various solvents. As always, addressing solubility is crucial for applications in synthesis and formulation.