Interesting facts
Interesting Facts About N-(4-nitrophenyl)acetamide
N-(4-nitrophenyl)acetamide is a fascinating compound due to its unique properties and diverse applications. Here are some intriguing aspects that highlight its significance in both chemical research and industry:
- Chemical Structure: This compound contains a nitro group, which is a powerful electron-withdrawing group, influencing its reactivity and chemical behavior. The presence of the acetamide moiety contributes to its characteristic functional properties.
- Applications in Synthesis: N-(4-nitrophenyl)acetamide is often utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its ability to form derivatives makes it a valuable compound in synthetic chemistry.
- Biological Activity: This compound has been studied for its potential biological activities, including antimicrobial and antitumor properties. Research continues to explore its mechanism of action and efficacy in medicinal chemistry.
- Analytical Chemistry: N-(4-nitrophenyl)acetamide can be used as a reactant in various analytical techniques, contributing to the detection and quantification of other compounds through colorimetric or spectrophotometric methods.
As with many nitro compounds, its chemistry reflects an exciting interplay between structure and function. Understanding compounds like N-(4-nitrophenyl)acetamide not only broadens our knowledge of organic chemistry but also opens avenues for innovation in product development.
In the words of renowned chemist Linus Pauling: "It is the responsibility of the scientist to understand their influence on the world." This highlights the importance of studying compounds such as N-(4-nitrophenyl)acetamide and their impact on society.
Synonyms
N-(4-Nitrophenyl)acetamide
4'-Nitroacetanilide
104-04-1
4-NITROACETANILIDE
P-Nitroacetanilide
N-Acetyl-4-nitroaniline
p-Acetamidonitrobenzene
p-Nitrophenylacetanilide
N-Acetyl-p-nitroaniline
Acetamide, N-(4-nitrophenyl)-
Acetanilide, p-nitro-
Acetanilide, 4'-nitro-
NSC 1315
CCRIS 5566
Acetic acid 4-nitroanilide
EINECS 203-169-0
AI3-01545
NSC-1315
MFCD00007303
PH3B066365
N-(4-Nitro-phenyl)-acetamide
P-NITROACETANILIDE [MI]
DTXSID5059290
UNII-PH3B066365
p-acetamino nitrobenzene
Maybridge1_001346
WLN: WNR DMV1
4-Nitroacetanilide, 98%
N-(p-Nitrophenyl)acetamide
4-(Acetylamino)nitrobenzene
N-Acetyl-4-nitrobenzenamine
1-Nitro-4-acetylaminobenzene
4\'-NITROACETANILIDE
N-(4-nitrophenyl)-acetamide
SCHEMBL642700
Acetamide,N-(4-nitrophenyl)-
CHEMBL131469
Acetanilide, 4'-nitro-(8CI)
DTXCID3032838
HMS545F04
NSC1315
AB9858
STK004304
AKOS003237246
FN71072
SY106175
DB-040507
CS-0128761
N0108
NS00023276
10.14272/NQRLPDFELNCFHW-UHFFFAOYSA-N
7E-925
doi:10.14272/NQRLPDFELNCFHW-UHFFFAOYSA-N
Q7041448
N-ACETYL-4-NITROANILINE; Acetanilide,4'-nitro; 4'-Nitroacetanilide
203-169-0
VYZ
Solubility of N-(4-nitrophenyl)acetamide
N-(4-nitrophenyl)acetamide is known for its interesting solubility profile, which is significantly influenced by its chemical structure. This compound exhibits the following characteristics regarding solubility:
Overall, the solubility behavior of N-(4-nitrophenyl)acetamide illustrates the significant role that both molecular structure and solvent polarity play in determining how well this compound can dissolve.