Interesting facts
Interesting Facts about N-(1,3-benzothiazol-2-yl)-3-oxo-butanamide
N-(1,3-benzothiazol-2-yl)-3-oxo-butanamide is a fascinating compound that has garnered attention in various fields, particularly in medicinal chemistry and pharmacology. Here are some intriguing aspects of this compound:
- Unique Structure: This compound features a benzothiazole moiety, which is known for its diverse biological activities. The fusion of the benzene and thiazole rings grants it notable properties.
- Biological Relevance: Compounds containing benzothiazole derivatives often exhibit significant antimicrobial and anticancer activities, making them valuable in drug discovery. Researchers are actively exploring their potential as therapeutic agents.
- Reactive Functional Groups: The presence of the oxo and amide functional groups enhances its reactivity, suggesting potential for further chemical modifications. Such modifications could lead to the synthesis of novel derivatives with improved pharmacological profiles.
- Applications in Industry: Beyond its medicinal applications, compounds similar to this one are often used in agriculture and materials science. This versatility highlights its importance across different sectors.
- Research Tools: In laboratory settings, this compound can serve as a tool in biological assays to study various pathways and mechanisms within cellular systems.
In summary, N-(1,3-benzothiazol-2-yl)-3-oxo-butanamide is not just another chemical compound; it represents the intersection of structural innovation and biological potential. As the saying goes, "Chemistry is the art of problem-solving," and compounds like this are crucial in the quest for new solutions in healthcare and beyond.
Synonyms
4692-94-8
N-(2-Benzothiazolyl)-acetoacetamide
ACETOACETAMIDE, N-(2-BENZOTHIAZOLYL)-
2-(Acetoacetamido)benzothiazole
Butanamide, N-2-benzothiazolyl-3-oxo-
6LYP4R9QY6
NSC 86136
BRN 0202998
NSC-86136
DTXSID70196984
4-27-00-04845 (Beilstein Handbook Reference)
N-2-BENZOTHIAZOLYL-3-OXOBUTANAMIDE
ACETOACETAMIDE, N-2-BENZOTHIAZOLYL-
DTXCID10119475
Butanamide, N-2-benzothiazolyl-3-oxo-(9CI)
654-554-9
N-(1,3-benzothiazol-2-yl)-3-oxobutanamide
N-(Benzo[d]thiazol-2-yl)-3-oxobutanamide
N-(2-Benzothiazolyl)acetoacetamide
NSC86136
UNII-6LYP4R9QY6
SCHEMBL3933070
WLN: T56 BN DSJ CMV1V1
STK847135
AKOS000186887
AKOS005627043
N-(2-benzothiazolyl)-3-oxobutanamide
DB-031104
CS-0362366
N-[(2E)-1,3-benzothiazol-2(3H)-ylidene]-3-oxobutanamide
Solubility of N-(1,3-benzothiazol-2-yl)-3-oxo-butanamide
The solubility of the compound N-(1,3-benzothiazol-2-yl)-3-oxo-butanamide can be influenced by several factors, including its molecular structure and the nature of solvents used. Typically, this compound features a significant degree of polarity due to its functional groups, which tend to enhance its solubility in polar solvents.
Here are some key points regarding its solubility:
In conclusion, the solubility of N-(1,3-benzothiazol-2-yl)-3-oxo-butanamide may be quite variable, reflecting the complex interplay between its chemical structure and the solvent characteristics. Understanding these aspects is vital for applications in pharmaceuticals and chemical research, as solubility directly impacts bioavailability and reactivity.