4-Amino-1-cbz-piperidine-4-carboxylic acid
95%
- Product Code: 39729
CAS:
115655-41-9
| Molecular Weight: | 278.3037 g./mol | Molecular Formula: | C₁₄H₁₈N₂O₄ |
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| EC Number: | MDL Number: | MFCD03425218 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
4-Amino-1-cbz-piperidine-4-carboxylic acid is primarily utilized in organic synthesis as a key intermediate in the production of pharmaceuticals and bioactive compounds. Its structure, featuring both amino and carboxylic acid functional groups, makes it a versatile building block for the development of complex molecules. It is often employed in the synthesis of piperidine-based drugs, which are commonly used in the treatment of neurological disorders, pain management, and other therapeutic areas. Additionally, the CBz (carbobenzyloxy) protecting group allows for selective reactions, enabling the precise construction of target molecules in multi-step synthetic processes. This compound is particularly valuable in medicinal chemistry research for designing and optimizing drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $320.04 |
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4-Amino-1-cbz-piperidine-4-carboxylic acid
4-Amino-1-cbz-piperidine-4-carboxylic acid is primarily utilized in organic synthesis as a key intermediate in the production of pharmaceuticals and bioactive compounds. Its structure, featuring both amino and carboxylic acid functional groups, makes it a versatile building block for the development of complex molecules. It is often employed in the synthesis of piperidine-based drugs, which are commonly used in the treatment of neurological disorders, pain management, and other therapeutic areas. Additionally, the CBz (carbobenzyloxy) protecting group allows for selective reactions, enabling the precise construction of target molecules in multi-step synthetic processes. This compound is particularly valuable in medicinal chemistry research for designing and optimizing drug candidates.
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