tert-Butyl (2-bromo-5-methoxyphenyl)carbamate
≥95%
- Product Code: 121409
CAS:
169303-80-4
| Molecular Weight: | 302.16 g./mol | Molecular Formula: | C₁₂H₁₆BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11975638 | |
| Melting Point: | Boiling Point: | 316.7±32.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex compounds. Its structure, featuring a bromo and methoxy substituent on the phenyl ring, makes it a valuable building block in the development of pharmaceuticals and agrochemicals. The tert-butyl carbamate group serves as a protective group for amines, enabling selective reactions in multi-step synthetic processes. Additionally, it can be used in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active molecules. Its applications extend to the synthesis of potential drug candidates, particularly in the fields of oncology and neurology, where such aromatic frameworks are often explored.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft35,392.94 |
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| 1.000 | 10-20 days | Ft87,852.08 |
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| 5.000 | 10-20 days | Ft264,719.83 |
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| 10.000 | 10-20 days | Ft441,587.59 |
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tert-Butyl (2-bromo-5-methoxyphenyl)carbamate
This chemical is primarily utilized in organic synthesis as an intermediate for the preparation of more complex compounds. Its structure, featuring a bromo and methoxy substituent on the phenyl ring, makes it a valuable building block in the development of pharmaceuticals and agrochemicals. The tert-butyl carbamate group serves as a protective group for amines, enabling selective reactions in multi-step synthetic processes. Additionally, it can be used in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active molecules. Its applications extend to the synthesis of potential drug candidates, particularly in the fields of oncology and neurology, where such aromatic frameworks are often explored.
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