Ethyl 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetate
98%
- Product Code: 123972
CAS:
1158970-52-5
Molecular Weight: | 432.33 g./mol | Molecular Formula: | C₁₉H₁₈BrN₃O₂S |
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EC Number: | MDL Number: | MFCD31692645 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a triazole ring and a bromo-substituted naphthalene moiety, makes it a valuable building block for developing potential therapeutic agents. Researchers often employ it in the design and optimization of compounds targeting specific enzymes or receptors, particularly in the context of anti-inflammatory, anticancer, or antimicrobial drug discovery. The thioether linkage and ester group in its structure also allow for further chemical modifications, enabling the creation of diverse derivatives with tailored pharmacological properties. Additionally, its unique chemical framework is explored in materials science for developing organic semiconductors or optoelectronic materials due to its potential electronic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿31,005.00 |
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0.250 | 10-20 days | ฿52,686.00 |
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Ethyl 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a triazole ring and a bromo-substituted naphthalene moiety, makes it a valuable building block for developing potential therapeutic agents. Researchers often employ it in the design and optimization of compounds targeting specific enzymes or receptors, particularly in the context of anti-inflammatory, anticancer, or antimicrobial drug discovery. The thioether linkage and ester group in its structure also allow for further chemical modifications, enabling the creation of diverse derivatives with tailored pharmacological properties. Additionally, its unique chemical framework is explored in materials science for developing organic semiconductors or optoelectronic materials due to its potential electronic properties.
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