Interesting facts
Exploring N-(5-oxo-2H-furan-2-yl)acetamide
N-(5-oxo-2H-furan-2-yl)acetamide is a fascinating compound that showcases the intriguing chemistry of furan derivatives. This compound is particularly notable for several reasons:
- Unique Structure: The presence of the furan ring highlights its potential reactivity and versatility as a chemical intermediate in organic synthesis.
- Bioactivity: Compounds containing a furan nucleus have been studied extensively for their biological activity, which might include antibacterial, antifungal, and anticancer properties.
- Synthetic Applications: N-(5-oxo-2H-furan-2-yl)acetamide can serve as a precursor in the synthesis of various pharmaceuticals, emphasizing its importance in medicinal chemistry.
- Research Potential: Ongoing research explores its derivatives, which may lead to the discovery of new therapeutic agents or materials.
As a student or researcher in chemistry, exploring N-(5-oxo-2H-furan-2-yl)acetamide allows for a deeper understanding of:
- The chemistry of heterocyclic compounds.
- The methodologies for synthesizing complex chemical structures.
- The role of functional groups in modulating the properties of organic molecules.
In summary, N-(5-oxo-2H-furan-2-yl)acetamide is not merely a chemical compound but a gateway to exploring the intricate relationships between structure, reactivity, and biological activity within organic chemistry. As stated by one researcher, “The true beauty of chemistry lies in its complexity and the connections that can be drawn between simple molecules.”
Synonyms
5-Acetamido-2(5)-furanone
YM5GCO381H
NSC 114350
NSC-114350
BRN 1680823
AI3-44725
N-(2,5-Dihydro-5-oxo-2-furanyl)acetamide
UNII-YM5GCO381H
DTXSID401017456
5-18-11-00344 (Beilstein Handbook Reference)
Crotonic acid, 4-acetamido-4-hyroxy-, gamma-lactone
ACETAMIDO-4-HYDROXY-2-BUTENOIC ACID-Y-LACTONE
methyl 13-((2S)-2-hydroxy-3,4-dimethyl-5-oxofuran-2-yl)tridecanoate
methyl 13-[(2S)-2-hydroxy-3,4-dimethyl-5-oxofuran-2-yl]tridecanoate
CHEBI:50523
DTXCID701475651
N-(5-oxo-2,5-dihydrofuran-2-yl)ethanimidic acid
2-b4O
2-BUTEN-4-OLIDE
2-Furanone
butenolide
crotonolactone
furan-2-one
HUSDLVGPEKVWAL-UHFFFAOYSA-N
16275-44-8
N-(5-oxo-2H-furan-2-yl)acetamide
5-Acetamido-Butenolide
ACETAMIDE, N-(2,5-DIHYDRO-5-OXO-2-FURANYL)-
2(5H)-Furanone, 5-acetamido-
Acetamide, N-(2,5-dihydro-5-oxo-2-furyl)-
2-Acetamido-2,5-dihydro-5-oxofuran
4-Acetamido-4-hydroxy-2-butenoic acid-.gamma.-lactone
4-acetamido-2-buten-4-olide
4-Acetamido-4-hydroxy-2-butenoic acid gamma-lactone
4-Acetamido-4-hydroxy-2-butenoic acid-gamma-lactone
5-Acetamide-Butenolide
WLN: T5VOYJ CUNV1
orb2564009
SCHEMBL17393675
Acetamide, N-(2,5-dihydro-5-oxo-2-furanyl)-, (from Fusarium nivale)
MFCD00236146
NSC114350
AKOS006272219
Acetamide,5-dihydro-5-oxo-2-furyl)-
BS-1481
HY-W402074
Acetamide,5-dihydro-5-oxo-2-furanyl)-
PD212908
DS-006271
NS00122085
Acetamide,n-(2,5-dihydro-5-oxo-2-furanyl)-
N-(5-Oxo-2,5-dihydro-2-furanyl)acetamide #
Q27294586
4-ACETAMIDO-4-HYDROXY-2-BUTENOIC ACID .GAMMA.-LACTONE
5-Acetamide-Butenolide; 4-Acetamido-4-hydroxy-2-butenoic acid g-lactone
Solubility of N-(5-oxo-2H-furan-2-yl)acetamide
N-(5-oxo-2H-furan-2-yl)acetamide is an intriguing compound with notable solubility characteristics. This compound exhibits solubility in a range of solvents, which can be attributed to its structural features and functional groups. Here are some points to consider regarding its solubility:
Overall, the solubility profile of N-(5-oxo-2H-furan-2-yl)acetamide makes it a versatile candidate for various applications, particularly in fields requiring precise solubility characteristics. As the saying goes, "solubility is the key to solution!"