(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate
97%
- Product Code: 71045
CAS:
128102-16-9
| Molecular Weight: | 334.41 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06410782 | |
| Melting Point: | Boiling Point: | 435.4°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure is valuable for constructing piperazine-based frameworks, which are common in many therapeutic agents. This chemical is often employed in medicinal chemistry research to develop compounds targeting neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it is utilized in asymmetric synthesis to create chiral molecules, which are crucial for the development of enantiomerically pure drugs. Its protective Boc group allows for selective reactions, making it a versatile building block in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,020.00 |
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| 0.250 | 10-20 days | ฿14,040.00 |
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(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate
(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure is valuable for constructing piperazine-based frameworks, which are common in many therapeutic agents. This chemical is often employed in medicinal chemistry research to develop compounds targeting neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it is utilized in asymmetric synthesis to create chiral molecules, which are crucial for the development of enantiomerically pure drugs. Its protective Boc group allows for selective reactions, making it a versatile building block in multi-step synthetic processes.
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