Interesting facts
Interesting Facts about N-(3-hydroxyphenyl)acetamide
N-(3-hydroxyphenyl)acetamide, commonly referred to as a derivative of acetaminophen, is a fascinating compound that has drawn the attention of both chemists and pharmacologists. Its unique structure imparts a variety of properties that are worthy of exploration. Here are some engaging aspects of this compound:
- Biological Relevance: The compound is a close relative of acetaminophen, an over-the-counter analgesic and antipyretic. This connection indicates potential for similar pharmacological actions.
- Structure-Activity Relationship (SAR): The presence of the 3-hydroxy group on the phenyl ring is crucial. It is believed to enhance the compound's ability to interact with various biological targets, which is often a subject of intense research.
- Research Avenue: Ongoing studies are investigating the various derivatives of N-(3-hydroxyphenyl)acetamide for their efficacy in treating conditions such as pain and inflammation. The modification of the acetamide group can lead to a range of therapeutic benefits.
- Pharmacokinetics: Understanding how this compound is metabolized in the body can provide insights into its safety and potential side effects, allowing for better drug design.
- Multifunctionality: The compound may exhibit antioxidant properties due to its hydroxy group, making it a candidate for studies into neuroprotective effects as well.
- Engagement with the Chemistry Community: The exploration of such derivatives has led to numerous discussions in scientific circles, fostering collaboration and innovation among researchers.
In summary, N-(3-hydroxyphenyl)acetamide stands as a compelling subject in the field of organic and medicinal chemistry. Its close ties to well-known pharmacological agents make it an intriguing candidate for further study and development. The benefits of understanding its properties extend beyond academic curiosity, holding potential for breakthroughs in medical applications.
Synonyms
3-Acetamidophenol
Metacetamol
621-42-1
N-(3-Hydroxyphenyl)acetamide
3'-Hydroxyacetanilide
N-Acetyl-m-aminophenol
Acetamide, N-(3-hydroxyphenyl)-
m-Acetamidophenol
Pedituss
Metalid
Pyrapap
Rystal
3-(Acetylamino)phenol
M-HYDROXYACETANILIDE
m-(Acetylamino)phenol
Metacetamolum
Acetanilide, 3'-hydroxy-
BS 749
3-(Acetylamino)-1-hydroxybenzene
Metacetamolo
Metacetamolo [DCIT]
Metacetamol [INN:BAN]
Metacetamolum [INN-Latin]
NSC 3990
CCRIS 4567
CHEBI:76987
NSC-3990
EINECS 210-687-0
BS-749
BRN 0907998
V942ZCN81H
DTXSID3022089
AI3-01929
BS 479
METACETAMOL [INN]
DTXCID202089
Metacetamolum (INN-Latin)
Metacetamol, 3-Acetamidophenol
3-acetoamidophenol
MEALID
N-ACETYL-3-HYDROXYANILINE
BS479
210-687-0
inchi=1/c8h9no2/c1-6(10)9-7-3-2-4-8(11)5-7/h2-5,11h,1h3,(h,9,10
3-Hydroxyacetanilide
MFCD00002263
Metacetamol;3'-Hydroxyacetanilide
NCGC00091423-02
m-Acetaminophenol
acetyl-2-aminophenol
CAS-621-42-1
SMR000568485
3-ACETAMINOPHENOL
UNII-V942ZCN81H
3-acetamido phenol
3-acetylaminophenol
Spectrum_000976
SpecPlus_000775
Spectrum2_000517
Spectrum3_001262
Spectrum4_000086
Spectrum5_000701
3-Acetamidophenol, 97%
CHEMBL9419
BSPBio_002824
KBioGR_000352
KBioSS_001456
SPECTRUM211175
MLS000881135
MLS000881183
MLS001065601
DivK1c_006871
SCHEMBL181254
SPBio_000473
KBio1_001815
KBio2_001456
KBio2_004024
KBio2_006592
KBio3_002324
N-(3-Hydroxy-phenyl)-acetamide
NSC3990
HMS1923M09
Pharmakon1600-00211175
HY-B1309
STR00900
Tox21_111130
Tox21_200252
BDBM50088436
CCG-39594
NSC755827
STK949035
3-Acetamidophenol, analytical standard
AKOS000442198
Tox21_111130_1
AB00216
NSC-755827
PS-4520
NCGC00091423-01
NCGC00091423-03
NCGC00091423-04
NCGC00091423-05
NCGC00091423-06
NCGC00091423-08
NCGC00257806-01
SBI-0052664.P002
CS-0013071
H0188
NS00005679
EN300-15588
AB00053402_07
m-Hydroxyacetanilide N-(3-Hydroxyphenyl)acetamide
N-(3-Hydroxyphenyl)acetamide (3-Acetamidophenol)
SR-01000864571
SR-01000864571-2
BRD-K16474819-001-02-1
BRD-K16474819-001-09-6
Q27146503
Z31717082
F3385-6275
Solubility of N-(3-hydroxyphenyl)acetamide
N-(3-hydroxyphenyl)acetamide, also known as 3-hydroxyacetanilide, exhibits interesting solubility properties that are worth noting. The compound's solubility can be influenced by several factors, leading to its behavior in various solvents:
It’s also important to note that solubility can be impacted by factors such as pH and the presence of other solutes. For instance, the ionization of the hydroxyl group can alter the solubility profile:
In summary, while N-(3-hydroxyphenyl)acetamide is soluble in polar solvents, its varying solubility under different conditions makes it an intriguing compound for further study in solvent interactions.