tert-butyl 4-(4-bromothiazol-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
95%
- Product Code: 46318
CAS:
1332301-87-7
| Molecular Weight: | 345.25528 g./mol | Molecular Formula: | C₁₃H₁₇BrN₂O₂S |
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| EC Number: | MDL Number: | MFCD29054205 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of bioactive compounds, including potential drug candidates. Its structure, featuring both a bromothiazole and a dihydropyridine moiety, makes it suitable for further functionalization through various chemical reactions, such as cross-coupling or cyclization processes. Additionally, it is employed in research settings to study the structure-activity relationships of thiazole and pyridine derivatives, which are often explored for their therapeutic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $73.26 |
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| 0.250 | 10-20 days | $143.15 |
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| 1.000 | 10-20 days | $466.08 |
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tert-butyl 4-(4-bromothiazol-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is particularly valuable in the pharmaceutical industry, where it serves as a building block for the synthesis of bioactive compounds, including potential drug candidates. Its structure, featuring both a bromothiazole and a dihydropyridine moiety, makes it suitable for further functionalization through various chemical reactions, such as cross-coupling or cyclization processes. Additionally, it is employed in research settings to study the structure-activity relationships of thiazole and pyridine derivatives, which are often explored for their therapeutic properties.
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