Interesting facts
Exploring N-(4-phenylazophenyl)acetamide
N-(4-phenylazophenyl)acetamide is a fascinating compound that belongs to the class of azo compounds, known for their vibrant colors and diverse applications. Here are some intriguing aspects of this compound:
- Azo Compounds: The presence of the azo group (-N=N-) is what gives many azo compounds their rich coloration, typically making them important in dye manufacturing. This characteristic can be explored for applications in textiles and various industries.
- Potential Applications: Besides its use in dye formulations, N-(4-phenylazophenyl)acetamide may also hold potential in pharmaceuticals, owing to the functional amide group which can interact with biological systems.
- Synthesis: The synthesis of this compound often involves coupling reactions that can require careful control of reaction conditions to ensure high yields and desired properties.
- Research Interest: Azo compounds, including N-(4-phenylazophenyl)acetamide, are subject to ongoing research, particularly in areas such as drug delivery systems and as indicators in analytical chemistry.
As researchers continue to explore the properties and applications of compounds like N-(4-phenylazophenyl)acetamide, one cannot help but appreciate the complexity and utility of organic chemistry in broadening our understanding of material science and medicinal applications.
In the words of the famed chemist, Linus Pauling, "The best way to have a good idea is to have a lot of ideas." The study of compounds such as this opens the door to endless possibilities for innovation and discovery in the chemical world.
Synonyms
4'-(Phenylazo)acetanilide
N-[4-(2-Phenyldiazenyl)phenyl]acetamide
N-(4-(2-Phenyldiazenyl)phenyl)acetamide
664-121-6
p-Acetamidoazobenzene
4-Acetylaminoazobenzene
4128-71-6
4'-Phenylazoacetanilide
N-(4-phenyldiazenylphenyl)acetamide
p-(Phenylazo)acetanilide
Acetamide, N-(4-(phenylazo)phenyl)-
N-(4-(phenyldiazenyl)phenyl)acetamide
PARA-ACETAMIDOAZOBENZENE
4-Acetamidoazobenzene
Acetanilide, 4'-(phenylazo)-
N-(4-Phenylazo-phenyl)-acetamide
N-[4-(phenyldiazenyl)phenyl]acetamide
MLS000557208
NSC-5974
Acetamide, N-[4-(phenylazo)phenyl]-
NSC-404299
SMR000174022
WLN: 1VMR DNUNR
Acetamide, N-[4-[(1E)-2-phenyldiazenyl]phenyl]-
p-Phenylazoacetanilide
NSC 5974
30808-70-9
NSC 404299
Acetanilide, 4'-phenylazo-
BRN 0747512
N-(4-(PHENYLAZO)PHENYL)ACETAMIDE
AI3-17603
(E)-4-Acetamidoazobenzene
CBDivE_002398
4-16-00-00468 (Beilstein Handbook Reference)
cid_20085
N-(4-phenylazophenyl)acetamide
BG6347T8EQ
CHEMBL311003
SCHEMBL1405622
(E)-4'-(Phenylazo)acetanilide
CHEMBL1483163
BDBM49555
NSC5974
WSHHPNYAXLDUTG-WUKNDPDISA-N
DTXSID501040901
HMS2524J21
N-(4-phenyldiazenylphenyl)ethanamide
CCG-44266
NSC404299
STK097358
AKOS000485856
AKOS030743044
Acetanilide, 4'-(phenylazo)-, (E)-
NCGC00245036-01
N-{4-[(E)-phenyldiazenyl]phenyl}acetamide
CS-0367819
Acetamide, N-[4-(2-phenyldiazenyl)phenyl]-
H40967
N-[4-[(1E)-2-Phenyldiazenyl]phenyl]acetamide
N-(4-[(E)-2-Phenyldiazenyl]phenyl)acetamide #
SR-01000634113-1
Z30293007
Solubility Overview of N-(4-phenylazophenyl)acetamide
N-(4-phenylazophenyl)acetamide, a compound characterized by its complex organic structure, presents unique solubility properties. Its solubility can be influenced by a variety of factors, including polarity, hydrogen bonding capabilities, and the presence of functional groups.
Solubility Characteristics
For those working with N-(4-phenylazophenyl)acetamide, it is essential to consider these solubility characteristics for effective utilization in various chemical processes. As with many compounds, "the solution to solubility lies in the choice of solvent." Understanding these nuances can greatly enhance applications in organic synthesis and material science.