(S)-Methyl 3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
98%
- Product Code: 60154
CAS:
266306-18-7
| Molecular Weight: | 358.23 g./mol | Molecular Formula: | C₁₅H₂₀BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14636392 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of chiral molecules, which are essential for creating drugs with specific therapeutic effects. Its structure, featuring a bromophenyl group and a tert-butoxycarbonyl (Boc) protected amino group, makes it valuable for peptide coupling reactions and the construction of complex organic molecules. Additionally, it is employed in medicinal chemistry research for designing and optimizing drug candidates, especially those targeting neurological and cardiovascular diseases. The chiral nature of the compound also makes it useful in asymmetric synthesis, ensuring the production of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,602.00 |
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| 0.250 | 10-20 days | ฿2,556.00 |
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| 1.000 | 10-20 days | ฿6,885.00 |
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(S)-Methyl 3-(4-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of chiral molecules, which are essential for creating drugs with specific therapeutic effects. Its structure, featuring a bromophenyl group and a tert-butoxycarbonyl (Boc) protected amino group, makes it valuable for peptide coupling reactions and the construction of complex organic molecules. Additionally, it is employed in medicinal chemistry research for designing and optimizing drug candidates, especially those targeting neurological and cardiovascular diseases. The chiral nature of the compound also makes it useful in asymmetric synthesis, ensuring the production of enantiomerically pure substances.
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