ethyl 2-((2,6-difluorobenzyl)(ethoxycarbonyl)amino)-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate
CAS 308831-94-9
CAS · 308831-94-9
Product Overview
ethyl 2-((2,6-difluorobenzyl)(ethoxycarbonyl)amino)-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance: | Yellow to white solid |
|---|---|
| Purity (HPLC): | 99% min |
| Water content: | 1.0% max |
| Maximum single impurity: | 0.5% max |
| Identification: | By HPLC: The retention time of the major peak of the sample solution corresponds to that of the standard solution |
Applications
This compound is primarily used in pharmaceutical and medicinal chemistry as an intermediate for the synthesis of bioactive molecules, including potential enzyme inhibitors, receptor modulators, or antimicrobial agents. Its nitrophenyl and fluorinated aromatic groups enhance molecular stability and biological activity, making it suitable for structure-activity relationship studies in drug development. In agrochemical research, it can serve as a building block for novel pesticides, herbicides, or fungicides, where the thiophene scaffold contributes to environmental stability and target specificity. It is also used in organic synthesis for functionalization studies, where the multiple reactive sites allow selective transformations such as nucleophilic substitutions, reductions, and ester modifications. Additionally, the compound is valuable in materials science research for designing conjugated molecules or functional organic materials with electronic or optical properties.
Benefits
The benefits of this compound include its structural versatility, high chemical reactivity, and potential biological activity. The thiophene core provides a stable and conjugated platform for modifications, while the nitrophenyl and fluorinated groups enable tuning of electronic properties and bioactivity. Its ester and carbamate functionalities allow selective chemical transformations, supporting multi-step synthesis of complex molecules. The compound's stability under standard laboratory conditions and compatibility with common organic solvents make it convenient for handling and reaction optimization. Overall, it facilitates the design and synthesis of advanced intermediates with enhanced pharmacological or agrochemical properties.
Conclusion
In summary, ethyl 2-((2,6-difluorobenzyl)(ethoxycarbonyl)amino)-4-methyl-5-(4-nitrophenyl)thiophene-3-carboxylate is a versatile thiophene-based intermediate used in pharmaceutical, agrochemical, and organic synthesis research. Its multifunctional structure enables selective chemical transformations, supports drug and pesticide development, and contributes to the design of functional materials. With its reactivity, stability, and potential biological activity, it serves as a valuable building block for creating complex, bioactive, and functionally advanced molecules.
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