1-Boc-4-(2-aminoethyl)piperazine
98%
- Product Code: 72286
CAS:
192130-34-0
Molecular Weight: | 229.32 g./mol | Molecular Formula: | C₁₁H₂₃N₃O₂ |
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EC Number: | MDL Number: | MFCD02683049 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, sealed |
Product Description:
This chemical is widely used in organic synthesis, particularly in the pharmaceutical industry, for the preparation of various drug intermediates. It serves as a key building block in the development of compounds with potential therapeutic applications, such as inhibitors, receptor antagonists, and enzyme modulators. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at other functional sites, making it valuable in multi-step synthetic processes. Additionally, it is employed in the synthesis of peptides and peptidomimetics, where its structure facilitates the introduction of specific functional groups. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry and drug discovery research.
Product Specification:
Test | Specification |
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APPEARANCE | Yellow Crystals or Liquid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
CARBON | 55.6 % 59.6 % |
NITROGEN | 17.7 % 19.0 % |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿1,000.00 |
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5.000 | 10-20 days | ฿3,360.00 |
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25.000 | 10-20 days | ฿13,320.00 |
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100.000 | 10-20 days | ฿49,180.00 |
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1-Boc-4-(2-aminoethyl)piperazine
This chemical is widely used in organic synthesis, particularly in the pharmaceutical industry, for the preparation of various drug intermediates. It serves as a key building block in the development of compounds with potential therapeutic applications, such as inhibitors, receptor antagonists, and enzyme modulators. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions at other functional sites, making it valuable in multi-step synthetic processes. Additionally, it is employed in the synthesis of peptides and peptidomimetics, where its structure facilitates the introduction of specific functional groups. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry and drug discovery research.
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