2-((4-Bromonaphthalen-1-yl)oxy)-N'-((5-nitrothiophen-2-yl)methylene)acetohydrazide
98%
- Product Code: 41152
CAS:
413606-16-3
| Molecular Weight: | 434.2639 g./mol | Molecular Formula: | C₁₇H₁₂BrN₃O₄S |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its potential biological activities. It is often studied for its antimicrobial and anticancer properties, as the structural components, such as the nitrothiophene and bromonaphthalene moieties, are known to exhibit significant pharmacological effects. Researchers explore its efficacy in inhibiting the growth of various bacterial and fungal strains, making it a candidate for developing new antimicrobial agents. Additionally, its potential to interact with specific cellular targets, such as enzymes or receptors, is investigated for designing novel anticancer therapies. The compound’s hydrazide linkage also contributes to its ability to act as a chelating agent, which can be useful in metal ion binding studies or as a precursor for synthesizing more complex bioactive molecules. Its applications extend to material science, where it may be used in the development of organic semiconductors or optoelectronic materials due to its conjugated aromatic system.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿35,010.00 |
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2-((4-Bromonaphthalen-1-yl)oxy)-N'-((5-nitrothiophen-2-yl)methylene)acetohydrazide
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its potential biological activities. It is often studied for its antimicrobial and anticancer properties, as the structural components, such as the nitrothiophene and bromonaphthalene moieties, are known to exhibit significant pharmacological effects. Researchers explore its efficacy in inhibiting the growth of various bacterial and fungal strains, making it a candidate for developing new antimicrobial agents. Additionally, its potential to interact with specific cellular targets, such as enzymes or receptors, is investigated for designing novel anticancer therapies. The compound’s hydrazide linkage also contributes to its ability to act as a chelating agent, which can be useful in metal ion binding studies or as a precursor for synthesizing more complex bioactive molecules. Its applications extend to material science, where it may be used in the development of organic semiconductors or optoelectronic materials due to its conjugated aromatic system.
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