tert-Butyl (5-bromothiazol-2-yl)(methyl)carbamate
95%
- Product Code: 87882
CAS:
1314095-64-1
| Molecular Weight: | 293.18 g./mol | Molecular Formula: | C₉H₁₃BrN₂O₂S |
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| EC Number: | MDL Number: | MFCD24469923 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate in the production of more complex molecules. Its structure, featuring a bromothiazole ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting various diseases. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Additionally, the thiazole moiety is often found in molecules with antimicrobial, anti-inflammatory, or anticancer properties, making this compound a key building block in medicinal chemistry. Its stability and reactivity also make it suitable for use in combinatorial chemistry and high-throughput screening processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft72,240.39 |
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tert-Butyl (5-bromothiazol-2-yl)(methyl)carbamate
This compound is primarily utilized in organic synthesis and pharmaceutical research as an intermediate in the production of more complex molecules. Its structure, featuring a bromothiazole ring and a tert-butyl carbamate group, makes it valuable for constructing biologically active compounds, particularly in the development of drugs targeting various diseases. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Additionally, the thiazole moiety is often found in molecules with antimicrobial, anti-inflammatory, or anticancer properties, making this compound a key building block in medicinal chemistry. Its stability and reactivity also make it suitable for use in combinatorial chemistry and high-throughput screening processes.
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