(S)-2-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)acetic acid
≥95%
- Product Code: 38621
CAS:
1228547-87-2
| Molecular Weight: | 330.17 g./mol | Molecular Formula: | C₁₃H₁₆BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07371725 | |
| Melting Point: | Boiling Point: | 456.3°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of chiral compounds, where its stereochemistry plays a crucial role in ensuring the desired biological activity of the final product. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions to occur at other functional sites, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients (APIs). Its bromophenyl moiety can also be leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to construct more elaborate structures. Overall, it is a versatile building block in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,368.00 |
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| 0.250 | 10-20 days | ฿20,745.00 |
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(S)-2-(2-Bromophenyl)-2-((tert-butoxycarbonyl)amino)acetic acid
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of chiral compounds, where its stereochemistry plays a crucial role in ensuring the desired biological activity of the final product. The tert-butoxycarbonyl (Boc) protecting group allows for selective reactions to occur at other functional sites, making it valuable in peptide synthesis and the development of active pharmaceutical ingredients (APIs). Its bromophenyl moiety can also be leveraged in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to construct more elaborate structures. Overall, it is a versatile building block in medicinal chemistry and drug discovery.
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