tert-Butyl ((2-bromothiazol-5-yl)methyl)carbamate
95%
- Product Code: 130660
CAS:
519003-04-4
| Molecular Weight: | 293.18 g./mol | Molecular Formula: | C₉H₁₃BrN₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20923801 | |
| Melting Point: | Boiling Point: | 382.3±25.0 °C(Predicted) | |
| Density: | 1.469±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure allows for selective functionalization at the thiazole ring and amine group after deprotection, making it valuable in building complex molecules. Commonly employed in the development of kinase inhibitors and antimicrobial agents. The bromine atom serves as a handle for cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification in medicinal chemistry campaigns. Also utilized in the preparation of labeled compounds for metabolic studies due to its stability and reactivity profile.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,440.00 |
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| 250mg | 10-20 days | ฿4,760.00 |
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| 1g | 10-20 days | ฿14,710.00 |
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tert-Butyl ((2-bromothiazol-5-yl)methyl)carbamate
Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its structure allows for selective functionalization at the thiazole ring and amine group after deprotection, making it valuable in building complex molecules. Commonly employed in the development of kinase inhibitors and antimicrobial agents. The bromine atom serves as a handle for cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification in medicinal chemistry campaigns. Also utilized in the preparation of labeled compounds for metabolic studies due to its stability and reactivity profile.
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