(R)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate
97%
- Product Code: 113420
CAS:
380610-92-4
| Molecular Weight: | 316.19 g./mol | Molecular Formula: | C₁₃H₁₈BrNO₃ |
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| EC Number: | MDL Number: | MFCD27978721 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing biologically active compounds, such as inhibitors or receptor modulators. The presence of the tert-butyl group enhances stability during synthetic processes, while the hydroxyl group provides a reactive site for further functionalization. It is often employed in the development of chiral drugs due to its (R)-configuration, which is crucial for achieving specific stereochemical outcomes in drug design. Additionally, the bromine atom serves as a handle for cross-coupling reactions, enabling the introduction of diverse substituents to tailor the compound's properties for targeted applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €18.76 |
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| 0.250 | 10-20 days | €31.34 |
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| 1.000 | 10-20 days | €93.55 |
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(R)-tert-Butyl (1-(3-bromophenyl)-2-hydroxyethyl)carbamate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules, particularly in the pharmaceutical industry. Its structure, featuring a bromophenyl group and a carbamate moiety, makes it valuable for constructing biologically active compounds, such as inhibitors or receptor modulators. The presence of the tert-butyl group enhances stability during synthetic processes, while the hydroxyl group provides a reactive site for further functionalization. It is often employed in the development of chiral drugs due to its (R)-configuration, which is crucial for achieving specific stereochemical outcomes in drug design. Additionally, the bromine atom serves as a handle for cross-coupling reactions, enabling the introduction of diverse substituents to tailor the compound's properties for targeted applications.
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