1-Cbz-3-ethylpiperidine-3-carboxylic Acid
≥97%
- Product Code: 76194
CAS:
1245808-57-4
Molecular Weight: | 291.34 g./mol | Molecular Formula: | C₁₆H₂₁NO₄ |
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EC Number: | MDL Number: | MFCD17976788 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, dry |
Product Description:
1-Cbz-3-ethylpiperidine-3-carboxylic acid is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds targeting neurological and psychiatric disorders. The Cbz (carbobenzyloxy) protecting group in the molecule is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective deprotection and further functionalization. This compound is also valuable in peptide chemistry, where it aids in the construction of peptide chains with specific structural features. Its versatility makes it a useful building block in medicinal chemistry research, enabling the creation of novel drug candidates with potential therapeutic applications.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿12,285.00 |
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5.000 | 10-20 days | ฿32,985.00 |
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1-Cbz-3-ethylpiperidine-3-carboxylic Acid
1-Cbz-3-ethylpiperidine-3-carboxylic acid is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds targeting neurological and psychiatric disorders. The Cbz (carbobenzyloxy) protecting group in the molecule is crucial for safeguarding the amine functionality during multi-step synthetic processes, allowing for selective deprotection and further functionalization. This compound is also valuable in peptide chemistry, where it aids in the construction of peptide chains with specific structural features. Its versatility makes it a useful building block in medicinal chemistry research, enabling the creation of novel drug candidates with potential therapeutic applications.
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