4-(6-Amino-3-pyridyl)-1-Boc-piperazine
99%
- Product Code: 46375
CAS:
571188-59-5
| Molecular Weight: | 278.35 g./mol | Molecular Formula: | C₁₄H₂₂N₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11594962 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃ |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of piperazine derivatives. Its structure, featuring a Boc-protected piperazine and an amino-pyridyl group, makes it valuable for constructing complex molecules, especially in drug discovery programs targeting central nervous system disorders, cancer, and infectious diseases. Researchers often employ it in the preparation of small molecule inhibitors, receptor ligands, and other pharmacologically relevant compounds. Additionally, its protective group allows for selective deprotection and further functionalization, enhancing its versatility in multi-step synthetic routes.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 99-100 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿300.00 |
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| 1.000 | 10-20 days | ฿400.00 |
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| 5.000 | 10-20 days | ฿700.00 |
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| 25.000 | 10-20 days | ฿1,500.00 |
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| 100.000 | 10-20 days | ฿4,250.00 |
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4-(6-Amino-3-pyridyl)-1-Boc-piperazine
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of piperazine derivatives. Its structure, featuring a Boc-protected piperazine and an amino-pyridyl group, makes it valuable for constructing complex molecules, especially in drug discovery programs targeting central nervous system disorders, cancer, and infectious diseases. Researchers often employ it in the preparation of small molecule inhibitors, receptor ligands, and other pharmacologically relevant compounds. Additionally, its protective group allows for selective deprotection and further functionalization, enhancing its versatility in multi-step synthetic routes.
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