(R)-1-Boc-Piperazine-2-carboxylic acid
97%
- Product Code: 230099
CAS:
278788-60-6
| Molecular Weight: | 230.26 g./mol | Molecular Formula: | C₁₀H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179106 | |
| Melting Point: | 243-247°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 Boc-protected piperazine ring allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, metabolic diseases, and oncology due to the prevalence of piperazine motifs in bioactive molecules. The carboxylic acid group enables coupling reactions with amines to form amide bonds, facilitating the construction of complex molecular architectures in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $68.41 |
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| 1.000 | 10-20 days | $135.98 |
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| 5.000 | 10-20 days | $504.39 |
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| 25.000 | 10-20 days | $2,186.69 |
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(R)-1-Boc-Piperazine-2-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 Boc-protected piperazine ring allows for selective deprotection and further functionalization, making it valuable in multi-step organic synthesis. Commonly employed in the preparation of drug candidates targeting central nervous system disorders, metabolic diseases, and oncology due to the prevalence of piperazine motifs in bioactive molecules. The carboxylic acid group enables coupling reactions with amines to form amide bonds, facilitating the construction of complex molecular architectures in medicinal chemistry research.
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