(R)-1-Boc-Piperazine-3-carboxylic acid
97%
- Product Code: 230098
CAS:
192330-11-3
| Molecular Weight: | 230.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 231-239°C | Boiling Point: | 371.8°C |
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group and carboxylic acid functionality allow for selective coupling reactions, making it valuable in peptide-like structures and heterocyclic compounds. Commonly employed in medicinal chemistry for drug discovery programs targeting central nervous system disorders, metabolic diseases, and oncology due to its structural compatibility with bioactive molecules. The Boc-protected piperazine ring enhances solubility and stability during synthetic transformations, facilitating multi-step syntheses in both solution and solid-phase formats.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿620.00 |
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| 1g | 10-20 days | ฿1,880.00 |
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| 5g | 10-20 days | ฿8,480.00 |
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| 10g | 10-20 days | ฿16,800.00 |
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| 25g | 10-20 days | ฿36,800.00 |
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(R)-1-Boc-Piperazine-3-carboxylic acid
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group and carboxylic acid functionality allow for selective coupling reactions, making it valuable in peptide-like structures and heterocyclic compounds. Commonly employed in medicinal chemistry for drug discovery programs targeting central nervous system disorders, metabolic diseases, and oncology due to its structural compatibility with bioactive molecules. The Boc-protected piperazine ring enhances solubility and stability during synthetic transformations, facilitating multi-step syntheses in both solution and solid-phase formats.
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