tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
95%
- Product Code: 113008
CAS:
1086391-99-2
| Molecular Weight: | 300.19 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11506015 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a building block or intermediate in the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs) due to its carbamate and bromophenyl functional groups, which allow for further chemical modifications. The tert-butyl group provides steric protection, enabling selective reactions at other sites of the molecule. Additionally, it can be employed in the synthesis of agrochemicals and fine chemicals, where its structural features contribute to the creation of compounds with specific biological activities. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also noteworthy, as it facilitates the formation of carbon-carbon or carbon-nitrogen bonds, essential in constructing diverse organic frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,500.00 |
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| 0.250 | 10-20 days | ฿7,542.00 |
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| 1.000 | 10-20 days | ฿19,521.00 |
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tert-Butyl (1-(2-bromophenyl)ethyl)carbamate
This compound is primarily utilized in organic synthesis as a building block or intermediate in the preparation of more complex molecules. It is particularly valuable in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs) due to its carbamate and bromophenyl functional groups, which allow for further chemical modifications. The tert-butyl group provides steric protection, enabling selective reactions at other sites of the molecule. Additionally, it can be employed in the synthesis of agrochemicals and fine chemicals, where its structural features contribute to the creation of compounds with specific biological activities. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, is also noteworthy, as it facilitates the formation of carbon-carbon or carbon-nitrogen bonds, essential in constructing diverse organic frameworks.
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