1-Boc-3,3-Dimethylpiperazine
98%
- Product Code: 146626
CAS:
259808-67-8
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07371651 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily as a building block in organic synthesis, especially in the pharmaceutical industry. It serves as a protected form of 3,3-dimethylpiperazine, allowing selective reactions at other sites in the molecule without interference from the piperazine nitrogen. Commonly employed in the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of kinase inhibitors, antiviral agents, and central nervous system drugs. Its Boc (tert-butoxycarbonyl) protection group is easily removed under mild acidic conditions, making it ideal for multi-step syntheses where controlled deprotection is required. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the steric and electronic properties imparted by the dimethyl and Boc groups.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,220.00 |
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| 5.000 | 10-20 days | ฿5,440.00 |
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| 10.000 | 10-20 days | ฿10,790.00 |
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| 25.000 | 10-20 days | ฿23,400.00 |
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1-Boc-3,3-Dimethylpiperazine
Used primarily as a building block in organic synthesis, especially in the pharmaceutical industry. It serves as a protected form of 3,3-dimethylpiperazine, allowing selective reactions at other sites in the molecule without interference from the piperazine nitrogen. Commonly employed in the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of kinase inhibitors, antiviral agents, and central nervous system drugs. Its Boc (tert-butoxycarbonyl) protection group is easily removed under mild acidic conditions, making it ideal for multi-step syntheses where controlled deprotection is required. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to the steric and electronic properties imparted by the dimethyl and Boc groups.
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| Stable in pH range | - |
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