Methyl N-Cbz-3-piperidinecarboxylate
≥97%
- Product Code: 76513
CAS:
174543-74-9
| Molecular Weight: | 277.32 g./mol | Molecular Formula: | C₁₅H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06795953 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Methyl N-Cbz-3-piperidinecarboxylate is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various bioactive compounds and active pharmaceutical ingredients (APIs). The compound is often utilized in the synthesis of piperidine derivatives, which are essential in the development of drugs targeting the central nervous system, including antipsychotics, analgesics, and anticonvulsants. Its N-Cbz (carbobenzyloxy) protecting group allows for selective deprotection, enabling precise control over the synthetic pathway. Additionally, it is employed in peptide chemistry for the modification of amino acids and peptides, enhancing their stability and bioavailability. The ester functionality in the molecule also makes it a versatile building block for further chemical transformations, such as hydrolysis or reduction, to yield desired products for medicinal chemistry applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿657.00 |
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| 25.000 | 10-20 days | ฿1,170.00 |
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Methyl N-Cbz-3-piperidinecarboxylate
Methyl N-Cbz-3-piperidinecarboxylate is widely used in organic synthesis, particularly in the pharmaceutical industry. It serves as a key intermediate in the preparation of various bioactive compounds and active pharmaceutical ingredients (APIs). The compound is often utilized in the synthesis of piperidine derivatives, which are essential in the development of drugs targeting the central nervous system, including antipsychotics, analgesics, and anticonvulsants. Its N-Cbz (carbobenzyloxy) protecting group allows for selective deprotection, enabling precise control over the synthetic pathway. Additionally, it is employed in peptide chemistry for the modification of amino acids and peptides, enhancing their stability and bioavailability. The ester functionality in the molecule also makes it a versatile building block for further chemical transformations, such as hydrolysis or reduction, to yield desired products for medicinal chemistry applications.
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