Interesting facts
Interesting Facts About N-(4-allyloxyphenyl)acetamide
N-(4-allyloxyphenyl)acetamide is a fascinating compound that sits at the intersection of organic chemistry and medicinal research. Here are some intriguing aspects of this compound:
- Chemical Structure: This compound features an acetamide group attached to a phenyl ring, which is further substituted with an allyloxy group. This unique structure plays a significant role in its potential biological activities.
- Applications in Drug Development: Researchers are exploring the possibility of N-(4-allyloxyphenyl)acetamide as a lead compound in the development of pharmaceutical agents. Its structural motifs can be strategically modified to optimize efficacy and reduce toxicity.
- Biological Activity: Although comprehensive studies are still ongoing, preliminary research has indicated that derivatives of this compound may exhibit anti-inflammatory and analgesic properties, making it a candidate for pain management therapies.
- Synthetic Pathway: The synthesis of N-(4-allyloxyphenyl)acetamide often involves techniques such as nucleophilic substitution and acylation, showcasing prowess in synthetic organic chemistry.
- Interdisciplinary Importance: This compound is not only of interest to chemists but also to biologists and pharmacologists, highlighting the interdisciplinary nature of modern scientific inquiry.
As research progresses, N-(4-allyloxyphenyl)acetamide may reveal even more secrets and applications, which could pave the way for new therapeutic solutions. Stay tuned for further developments in this intriguing chemical landscape!
Synonyms
6622-73-7
4-Allyloxyacetanilide
4'-Allyloxyacetanilide
ACETANILIDE, 4'-ALLYLOXY-
4'-(Allyloxy)acetanilide
EINECS 229-573-7
QX9NI4B2O6
NSC 55077
BRN 3256889
NSC-55077
UNII-QX9NI4B2O6
DTXSID30216415
4'-(ALLYLOXY)-ACETANILIDE
4-13-00-01096 (Beilstein Handbook Reference)
4-ACETAMIDOPHENYL ALLYL ETHER
4-ACETAMIDO-1-ALLYLOXYBENZENE
ALLYL P-(ACETYLAMINO)PHENYL ETHER
N-(4-(2-PROPENYLOXY)PHENYL)ACETAMIDE
N-(4-(2-PROPENYLOXY)PHENYL)-ACETAMIDE
N-(4-(2-PROPEN-1-YLOXY)PHENYL)ACETAMIDE
N-[4-(2-Propen-1-yloxy)phenyl]acetamide
DTXCID30138906
229-573-7
N1-[4-(allyloxy)phenyl]acetamide
N-(4-prop-2-enoxyphenyl)acetamide
N-[4-(prop-2-en-1-yloxy)phenyl]acetamide
N-(4-(Allyloxy)phenyl)acetamide
N-[4-(allyloxy)phenyl]acetamide
NSC55077
MFCD00127763
4-Allyioxyacetanilide
Maybridge1_000059
p-Acetaminophenolallylather
MixCom1_000103
4-acetamido-1-allyloxy benzene
SCHEMBL7922185
CHEBI:194994
GAA62273
STL032680
AKOS000499228
NCGC00326257-01
TS-00257
DB-054887
CS-0236203
NS00035982
AB01320860-02
EN300-1697104
Solubility of N-(4-allyloxyphenyl)acetamide
N-(4-allyloxyphenyl)acetamide, known for its intriguing structural properties, exhibits notable characteristics when it comes to solubility.
Here are some key points regarding its solubility:
In summary, the solubility of N-(4-allyloxyphenyl)acetamide is significantly influenced by the polarity of the solvent used. Its ability to engage in hydrogen bonding plays a crucial role in determining how well it dissolves in various media. Thus, as with many chemical compounds, selecting the appropriate solvent is key to effectively utilizing this compound in various applications.