Methyl 1-Boc-5-Hydroxypiperidine-3-carboxylate
≥95%
- Product Code: 76200
CAS:
1095010-47-1
| Molecular Weight: | 259.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11656770 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its applications include:
1. **Pharmaceutical Research**: It serves as a key building block in the synthesis of various drug candidates, particularly those targeting neurological and cardiovascular diseases. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, enabling the creation of specific pharmacophores.
2. **Peptide Chemistry**: It is utilized in the synthesis of modified peptides, where the hydroxyl and carboxyl groups can be further functionalized to introduce specific structural or functional properties.
3. **Chemical Biology**: The compound is employed in the development of probes and inhibitors for studying biological pathways, leveraging its ability to mimic natural structures.
4. **Material Science**: It can be used in the design of novel polymers or coatings, where its functional groups contribute to the material's properties, such as adhesion or biocompatibility.
5. **Agrochemical Development**: It acts as an intermediate in the synthesis of pesticides or herbicides, where its structural features are modified to enhance efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,863.00 |
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| 1.000 | 10-20 days | ฿4,509.00 |
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Methyl 1-Boc-5-Hydroxypiperidine-3-carboxylate
This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its applications include:
1. **Pharmaceutical Research**: It serves as a key building block in the synthesis of various drug candidates, particularly those targeting neurological and cardiovascular diseases. The Boc (tert-butoxycarbonyl) protecting group allows for selective reactions, enabling the creation of specific pharmacophores.
2. **Peptide Chemistry**: It is utilized in the synthesis of modified peptides, where the hydroxyl and carboxyl groups can be further functionalized to introduce specific structural or functional properties.
3. **Chemical Biology**: The compound is employed in the development of probes and inhibitors for studying biological pathways, leveraging its ability to mimic natural structures.
4. **Material Science**: It can be used in the design of novel polymers or coatings, where its functional groups contribute to the material's properties, such as adhesion or biocompatibility.
5. **Agrochemical Development**: It acts as an intermediate in the synthesis of pesticides or herbicides, where its structural features are modified to enhance efficacy and selectivity.
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