tert-Butyl 4-bromobenzyl(methyl)carbamate
95%
- Product Code: 47584
CAS:
260809-26-5
| Molecular Weight: | 300.2000 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₂ |
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| EC Number: | MDL Number: | MFCD09701229 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require a bromobenzyl moiety. Its tert-butyl carbamate group provides protection for amines during multi-step reactions, ensuring selective transformations without unwanted side reactions. Additionally, it is employed in research settings for the study of enzyme inhibitors and receptor modulators, where the bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its stability and reactivity make it a valuable tool in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £83.46 |
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tert-Butyl 4-bromobenzyl(methyl)carbamate
This chemical is primarily utilized in organic synthesis as a building block for the preparation of more complex molecules. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that require a bromobenzyl moiety. Its tert-butyl carbamate group provides protection for amines during multi-step reactions, ensuring selective transformations without unwanted side reactions. Additionally, it is employed in research settings for the study of enzyme inhibitors and receptor modulators, where the bromine atom allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its stability and reactivity make it a valuable tool in medicinal chemistry and drug discovery processes.
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