tert-Butyl (2-(bromomethyl)phenyl)carbamate
96%
- Product Code: 36329
CAS:
166329-43-7
| Molecular Weight: | 286.16 g./mol | Molecular Formula: | C₁₂H₁₆BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11616720 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
tert-Butyl (2-(bromomethyl)phenyl)carbamate is primarily used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure, featuring both a carbamate group and a bromomethyl group, makes it a versatile building block for constructing complex molecules. The bromomethyl group is highly reactive, enabling it to participate in nucleophilic substitution reactions, which are crucial for forming carbon-carbon or carbon-heteroatom bonds. This compound is often employed in the synthesis of drug candidates, especially those targeting neurological disorders or cancer, due to its ability to introduce functional groups that enhance binding affinity or modulate biological activity. Additionally, it is utilized in the development of peptide mimetics and other bioactive molecules, where the tert-butyl group provides steric protection during synthetic processes. Its applications extend to materials science, where it can be used to modify polymers or create specialized coatings with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,384.00 |
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tert-Butyl (2-(bromomethyl)phenyl)carbamate
tert-Butyl (2-(bromomethyl)phenyl)carbamate is primarily used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure, featuring both a carbamate group and a bromomethyl group, makes it a versatile building block for constructing complex molecules. The bromomethyl group is highly reactive, enabling it to participate in nucleophilic substitution reactions, which are crucial for forming carbon-carbon or carbon-heteroatom bonds. This compound is often employed in the synthesis of drug candidates, especially those targeting neurological disorders or cancer, due to its ability to introduce functional groups that enhance binding affinity or modulate biological activity. Additionally, it is utilized in the development of peptide mimetics and other bioactive molecules, where the tert-butyl group provides steric protection during synthetic processes. Its applications extend to materials science, where it can be used to modify polymers or create specialized coatings with tailored properties.
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