(S)-4-(2-Bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid
98%
- Product Code: 60727
CAS:
403661-78-9
| Molecular Weight: | 358.23 g./mol | Molecular Formula: | C₁₅H₂₀BrNO₄ |
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| EC Number: | MDL Number: | MFCD03788796 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in the pharmaceutical industry. It serves as a building block for the development of active pharmaceutical ingredients (APIs), especially those targeting neurological and cardiovascular diseases. Its structure, featuring a bromophenyl group and a tert-butoxycarbonyl (Boc) protected amino group, makes it valuable for peptide coupling reactions and the synthesis of chiral compounds. Additionally, it is employed in research settings for the study of enzyme inhibitors and receptor modulators, contributing to the development of novel therapeutic agents. Its role in asymmetric synthesis also highlights its importance in creating enantiomerically pure drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,362.00 |
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| 0.250 | 10-20 days | ฿11,025.00 |
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| 1.000 | 10-20 days | ฿27,558.00 |
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(S)-4-(2-Bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid
This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in the pharmaceutical industry. It serves as a building block for the development of active pharmaceutical ingredients (APIs), especially those targeting neurological and cardiovascular diseases. Its structure, featuring a bromophenyl group and a tert-butoxycarbonyl (Boc) protected amino group, makes it valuable for peptide coupling reactions and the synthesis of chiral compounds. Additionally, it is employed in research settings for the study of enzyme inhibitors and receptor modulators, contributing to the development of novel therapeutic agents. Its role in asymmetric synthesis also highlights its importance in creating enantiomerically pure drugs.
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