tert-Butyl (5-bromo-2,3-difluorophenyl)carbamate
95%
- Product Code: 50161
CAS:
1150114-27-4
| Molecular Weight: | 308.1193 g./mol | Molecular Formula: | C₁₁H₁₂BrF₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12025956 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis as an intermediate for the development of pharmaceuticals and agrochemicals. Its structure, featuring a bromo and difluoro substitution on the phenyl ring, makes it valuable for further functionalization in drug discovery processes. The tert-butyl carbamate group provides protection for amines during multi-step synthetic routes, enabling the production of complex molecules. It is particularly useful in the synthesis of biologically active compounds targeting specific receptors or enzymes. Additionally, its halogenated aromatic ring can participate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create diverse chemical libraries for screening purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,886.00 |
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tert-Butyl (5-bromo-2,3-difluorophenyl)carbamate
Used primarily in organic synthesis as an intermediate for the development of pharmaceuticals and agrochemicals. Its structure, featuring a bromo and difluoro substitution on the phenyl ring, makes it valuable for further functionalization in drug discovery processes. The tert-butyl carbamate group provides protection for amines during multi-step synthetic routes, enabling the production of complex molecules. It is particularly useful in the synthesis of biologically active compounds targeting specific receptors or enzymes. Additionally, its halogenated aromatic ring can participate in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create diverse chemical libraries for screening purposes.
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