(3-Bromo-2-methyl-phenyl)-carbamic acid tert-butyl ester
97%
- Product Code: 36682
CAS:
221538-03-0
| Molecular Weight: | 286.1649 g./mol | Molecular Formula: | C₁₂H₁₆BrNO₂ |
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| EC Number: | MDL Number: | MFCD11975627 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical structures. It is often employed in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group serves as a protective group for the carbamic acid functionality. This protection allows for selective reactions to occur at other sites of the molecule without affecting the carbamic acid. Additionally, the bromine atom on the aromatic ring provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing diverse drug-like molecules. Its application is also seen in material science, where it can be used to modify polymers or create specialized coatings with specific properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $98.54 |
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(3-Bromo-2-methyl-phenyl)-carbamic acid tert-butyl ester
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex chemical structures. It is often employed in pharmaceutical research, particularly in the synthesis of active pharmaceutical ingredients (APIs) where the tert-butyl ester group serves as a protective group for the carbamic acid functionality. This protection allows for selective reactions to occur at other sites of the molecule without affecting the carbamic acid. Additionally, the bromine atom on the aromatic ring provides a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in constructing diverse drug-like molecules. Its application is also seen in material science, where it can be used to modify polymers or create specialized coatings with specific properties.
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