Interesting facts
Interesting Facts about N-(2-oxotetrahydrothiophen-3-yl)acetamide
N-(2-oxotetrahydrothiophen-3-yl)acetamide is a fascinating compound that captures interest for its unique structure and potential applications. Here are some noteworthy points to consider:
- Structural Characteristic: This compound contains a distinctive thiophene ring, which is known for its aromatic properties and plays an essential role in various biochemical processes.
- Biological Relevance: The presence of the acetamide group can enhance the biological activity of the compound, making it a candidate for pharmaceuticals, particularly in the development of new medications.
- Versatile Reactions: The 2-oxotetrahydrothiophen moiety suggests potential for interesting chemical reactions, especially in conjugation with other reagents, opening pathways in synthetic organic chemistry.
- Research Applications: Compounds like N-(2-oxotetrahydrothiophen-3-yl)acetamide may be studied for their anti-inflammatory and analgesic properties, contributing to pain management research.
- Interdisciplinary Appeal: This compound lies at the intersection of organic chemistry, medicinal chemistry, and materials science, appealing to a wide range of scientific disciplines.
As a summary, N-(2-oxotetrahydrothiophen-3-yl)acetamide stands out for its potential utility in medicinal applications and the intriguing chemistry stemming from its unique molecular framework. With ongoing research, the full scope of its capabilities may yet be discovered!
Synonyms
citiolone
1195-16-0
Citiolase
Thioxidrene
Ahctl
Acetamide, N-(tetrahydro-2-oxo-3-thienyl)-
Achtl
N-(2-oxothiolan-3-yl)acetamide
N-Acetylhomocysteine thiolactone
Citiolona
N-(TETRAHYDRO-2-OXO-3-THIENYL)ACETAMIDE
N-Acetyl-dl-homocysteine thiolactone
2-Acetamido-4-mercaptobutyric acid gamma-thiolactone
Citiolonum
Mucorex
Sitilon
N-Acetylhmocysteinethiolactone
Citiolone [INN:DCF]
BO 714
Citiolonum [INN-Latin]
Citiolona [INN-Spanish]
N-Acetylhomocysteinthiolakton
NSC 22878
alpha-Acetamido-gamma-thiobutyrolactone
2-Acetamido-4-mercaptobutyric acid thiolactone
UNII-70JKL15MUH
EINECS 214-793-8
EINECS 241-841-5
70JKL15MUH
Citiolone (INN)
NSC-22878
N-Acetylhomocysteinthiolakton [German]
BRN 0004338
DTXSID0045888
N-Acetyl-DL-homocystein thiolacton
CITIOLONE [INN]
CITIOLONE [MI]
CITIOLONE [MART.]
CITIOLONE [WHO-DD]
2-Thiolanone, 3-acetamido-
.alpha.-Acetamido-.gamma.-thiobutyrolactone
DTXCID8025888
(1)-N-(Tetrahydro-2-oxothien-3-yl)acetamide
dl-N-Acetylhomocysteinethiolactone
5-18-11-00320 (Beilstein Handbook Reference)
N-(2-Oxotetrahydro-3-thienyl)acetamide
cythiolone
Citiolonum (INN-Latin)
DL-3-(Acetylamino)tetrahydro-2-thiophenone
Citiolona (INN-Spanish)
CITIOLONE (MART.)
2-Acetamide-4-mercaptobutyric acid .gamma.-thiolactone
2-Acetamido-4-mercaptobutyric acid .gamma.-thiolactone
A05BA04
2-Acetamide-4-mercaptobutyric acid gamma-thiolactone
214-793-8
nrfjztxwlkpzav-uhfffaoysa-n
17896-21-8
DL-N-Acetylhomocysteine thiolactone
3-Acetamidotetrahydro-2-thiophenone
AHCT
N-(2-Oxotetrahydrothiophen-3-yl)acetamide
N-(TETRAHYDRO-2-OXO-3-THIENYL)-ACETAMIDE
SR-01000872700
N-(Tetrahydro-2-oxothienyl)acetamide
Prestwick_1
NCGC00016568-01
CAS-1195-16-0
MFCD00005480
Citiolone (Standard)
Prestwick0_000644
Prestwick1_000644
Prestwick2_000644
Prestwick3_000644
BSPBio_000647
SCHEMBL364495
SPBio_002568
BPBio1_000713
CHEMBL2104457
CHEBI:94403
HY-B0931R
N-(2-oxo-3-thiolanyl)acetamide
HMS1570A09
HMS2097A09
HMS3714A09
Pharmakon1600-01503205
BCP30727
HY-B0931
N-Acetyl-DL-homocystein Thiolactone
NSC22878
Tox21_111388
Tox21_113346
NSC758402
s4558
AKOS002808092
AKOS016162043
Tox21_113346_1
CCG-213865
DB13442
NSC-758402
NCGC00179491-01
NCGC00179491-04
AS-11951
DA-62350
DL-N-Acetylhomocysteine thiolactone, 98%
SBI-0207034.P001
DB-044348
A2144
NS00009177
D07105
EN300-100347
F17228
2-Acetamido-4-mercaptobutyric acid I(3)-thiolactone
SR-01000872700-1
SR-01000872700-2
BRD-A57957888-001-01-5
BRD-A57957888-001-06-4
BRD-A57957888-001-08-0
Q15408416
Acetamide, N-(tetrahydro-2-oxo-3-thienyl)-, (+/-)-
Acetamide, N-(tetrahydro-2-oxo-3-thienyl)-, (A+/-)-
Z995084668
Citiolase;Citiolona; Citiolonum; NSC 22878; NSC22878; NSC-22878
Solubility of N-(2-oxotetrahydrothiophen-3-yl)acetamide
N-(2-oxotetrahydrothiophen-3-yl)acetamide exhibits interesting solubility characteristics that depend on various factors such as polarity, molecular structure, and environmental conditions. Understanding the solubility of this compound can be crucial for practical applications including synthesis and formulation. Here are some key points to consider:
In laboratory settings, it has been observed that "solubility is often a key indicator of a compound's behavior in biological systems", which is particularly relevant for drug formulation and delivery. Understanding how N-(2-oxotetrahydrothiophen-3-yl)acetamide interacts with different solvents will aid researchers and manufacturers in harnessing its potential effectively.