Methyl 1-Boc-4-Aminopiperidine-4-carboxylate
≥95%
- Product Code: 76191
CAS:
321997-89-1
Molecular Weight: | 258.31 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₄ |
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EC Number: | MDL Number: | MFCD06200674 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in organic synthesis as an intermediate in the production of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a building block for the synthesis of complex molecules, especially those involving piperidine derivatives, which are common in drug design. The Boc (tert-butoxycarbonyl) protecting group in the compound allows for selective reactions, enabling chemists to modify specific parts of the molecule without affecting other functional groups. Its application is significant in the preparation of compounds targeting neurological disorders, cancer, and other therapeutic areas. Additionally, it is utilized in research laboratories for the development of novel drug candidates and in the study of chemical reactions involving piperidine structures.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿4,644.00 |
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1.000 | 10-20 days | ฿10,836.00 |
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Methyl 1-Boc-4-Aminopiperidine-4-carboxylate
This chemical is primarily used in organic synthesis as an intermediate in the production of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a building block for the synthesis of complex molecules, especially those involving piperidine derivatives, which are common in drug design. The Boc (tert-butoxycarbonyl) protecting group in the compound allows for selective reactions, enabling chemists to modify specific parts of the molecule without affecting other functional groups. Its application is significant in the preparation of compounds targeting neurological disorders, cancer, and other therapeutic areas. Additionally, it is utilized in research laboratories for the development of novel drug candidates and in the study of chemical reactions involving piperidine structures.
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