5-Bromo-N-isopropylthiophene-2-carboxamide
≥95%
- Product Code: 120223
CAS:
908494-87-1
| Molecular Weight: | 248.14 g./mol | Molecular Formula: | C₈H₁₀BrNOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08593344 | |
| Melting Point: | Boiling Point: | 336.881°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
5-Bromo-N-isopropylthiophene-2-carboxamide is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure is often leveraged in the creation of thiophene-based derivatives, which are known for their biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, this compound is employed in material science for the development of organic electronic materials, where thiophene derivatives are valued for their conductive and semiconductive properties. Researchers also use it in studies aimed at understanding structure-activity relationships to optimize drug candidates for improved efficacy and safety.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $62.83 |
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| 10.000 | 10-20 days | $89.50 |
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| 25.000 | 10-20 days | $114.82 |
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5-Bromo-N-isopropylthiophene-2-carboxamide
5-Bromo-N-isopropylthiophene-2-carboxamide is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. Its structure is often leveraged in the creation of thiophene-based derivatives, which are known for their biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. Additionally, this compound is employed in material science for the development of organic electronic materials, where thiophene derivatives are valued for their conductive and semiconductive properties. Researchers also use it in studies aimed at understanding structure-activity relationships to optimize drug candidates for improved efficacy and safety.
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