(S)-4-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid
98%
- Product Code: 60732
CAS:
270062-85-6
| Molecular Weight: | 358.23 g./mol | Molecular Formula: | C₁₅H₂₀BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861015 | |
| Melting Point: | Boiling Point: | 491.9℃°C at 767 mmHg | |
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target specific biological pathways. It serves as a key intermediate in the production of drugs that modulate neurotransmitter systems, potentially aiding in the treatment of neurological disorders such as depression, anxiety, or Parkinson's disease. Additionally, its structure, featuring a bromophenyl group and a protected amino acid moiety, makes it valuable in peptide chemistry for constructing complex peptide-based therapeutics. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling precise control during multi-step synthetic processes. This compound is also utilized in research settings for studying enzyme interactions and designing inhibitors for specific enzymes involved in disease mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £48.24 |
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| 0.250 | 10-20 days | £98.72 |
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| 1.000 | 10-20 days | £246.71 |
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(S)-4-(4-Bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid
This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) that target specific biological pathways. It serves as a key intermediate in the production of drugs that modulate neurotransmitter systems, potentially aiding in the treatment of neurological disorders such as depression, anxiety, or Parkinson's disease. Additionally, its structure, featuring a bromophenyl group and a protected amino acid moiety, makes it valuable in peptide chemistry for constructing complex peptide-based therapeutics. Its tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection, enabling precise control during multi-step synthetic processes. This compound is also utilized in research settings for studying enzyme interactions and designing inhibitors for specific enzymes involved in disease mechanisms.
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