R-1-Boc-3-methylpiperazine
97%
- Product Code: 121747
Alias:
R-(+)-1-Boc-3-methylpiperazine(R)-4-N-Boc-2-methylpiperazine
CAS:
163765-44-4
Molecular Weight: | 200.28 g./mol | Molecular Formula: | C₁₀H₂₀N₂O₂ |
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EC Number: | MDL Number: | MFCD02683205 | |
Melting Point: | 40-45 °C | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
R-1-Boc-3-methylpiperazine is widely used in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive compounds. Its primary application lies in the preparation of drug candidates, particularly in the development of central nervous system (CNS) drugs, antipsychotics, and other therapeutic agents. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, making it valuable in multi-step organic synthesis. Additionally, it is utilized in the creation of peptidomimetics and other complex molecules, where its structural framework contributes to the desired pharmacological properties. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry.
Product Specification:
Test | Specification |
---|---|
Purity (GC) | 97-100 |
Specific Rotation [A]20/D(C=1%, CHCL3) | 14-20 |
Appearance | Light Yellow Powder |
NMR | Conforms To Structure |
Note | This Product Is Low Melting Point Solid, May Change State In Different Environments (Solid, Liquid Or Semi-Solid) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿590.00 |
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25.000 | 10-20 days | ฿2,350.00 |
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100.000 | 10-20 days | ฿7,030.00 |
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R-1-Boc-3-methylpiperazine
R-1-Boc-3-methylpiperazine is widely used in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive compounds. Its primary application lies in the preparation of drug candidates, particularly in the development of central nervous system (CNS) drugs, antipsychotics, and other therapeutic agents. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, making it valuable in multi-step organic synthesis. Additionally, it is utilized in the creation of peptidomimetics and other complex molecules, where its structural framework contributes to the desired pharmacological properties. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry.
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