tert-Butyl (4-bromo-3-fluorophenyl)carbamate
≥97%
- Product Code: 82897
CAS:
868735-43-7
| Molecular Weight: | 290.13 g./mol | Molecular Formula: | C₁₁H₁₃BrFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11976284 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in pharmaceutical research and development, particularly in the synthesis of compounds with potential therapeutic properties. The presence of both bromo and fluoro substituents makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are common in drug discovery. Additionally, the tert-butyl carbamate group serves as a protective group for amines, enabling selective reactions in multi-step synthetic processes. Its application is crucial in the design and production of bioactive molecules, including those targeting specific enzymes or receptors in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,491.00 |
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| 1.000 | 10-20 days | ฿9,000.00 |
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| 5.000 | 10-20 days | ฿35,820.00 |
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tert-Butyl (4-bromo-3-fluorophenyl)carbamate
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. It is often employed in pharmaceutical research and development, particularly in the synthesis of compounds with potential therapeutic properties. The presence of both bromo and fluoro substituents makes it valuable for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are common in drug discovery. Additionally, the tert-butyl carbamate group serves as a protective group for amines, enabling selective reactions in multi-step synthetic processes. Its application is crucial in the design and production of bioactive molecules, including those targeting specific enzymes or receptors in medicinal chemistry.
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