(S)-4-Bromo-2-((tert-butoxycarbonyl)amino)pent-4-enoic acid
≥98%
- Product Code: 38528
CAS:
151215-34-8
| Molecular Weight: | 294.14 g./mol | Molecular Formula: | C₁₀H₁₆BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01320852 | |
| Melting Point: | Boiling Point: | 396.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of peptide-based drugs due to its ability to introduce specific functional groups into peptide chains. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Additionally, the presence of the bromoalkene moiety makes it a versatile building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in medicinal chemistry to create diverse drug candidates. Its application is particularly valuable in the synthesis of bioactive compounds targeting various diseases.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,198.00 |
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| 0.250 | 10-20 days | ฿15,093.00 |
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| 1.000 | 10-20 days | ฿26,469.00 |
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(S)-4-Bromo-2-((tert-butoxycarbonyl)amino)pent-4-enoic acid
This chemical is primarily used in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of peptide-based drugs due to its ability to introduce specific functional groups into peptide chains. The tert-butoxycarbonyl (Boc) protecting group in the compound is crucial for safeguarding the amino group during synthetic processes, allowing for selective reactions to occur elsewhere in the molecule. Additionally, the presence of the bromoalkene moiety makes it a versatile building block for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in medicinal chemistry to create diverse drug candidates. Its application is particularly valuable in the synthesis of bioactive compounds targeting various diseases.
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