4-(((tert-Butoxycarbonyl)amino)methyl)tetrahydro-2H-pyran-4-carboxylic acid
97%
- Product Code: 66013
CAS:
946761-11-1
| Molecular Weight: | 259.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₅ |
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| EC Number: | MDL Number: | MFCD09264199 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, avoid light, store in inert gas |
Product Description:
This compound is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a protected intermediate in organic synthesis, particularly in the construction of complex molecules. The tert-butoxycarbonyl (Boc) group provides stability during reactions, allowing selective deprotection when needed. It is often employed in the development of pharmaceuticals, where precise control over molecular structure is critical. Additionally, it can be utilized in the preparation of drug candidates targeting neurological or metabolic disorders, owing to its ability to introduce specific functional groups into a molecule. Its tetrahydropyran ring structure also contributes to its use in creating compounds with enhanced bioavailability and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,860.00 |
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| 0.250 | 10-20 days | ฿7,110.00 |
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4-(((tert-Butoxycarbonyl)amino)methyl)tetrahydro-2H-pyran-4-carboxylic acid
This compound is primarily used in the synthesis of peptides and other biologically active molecules. It serves as a protected intermediate in organic synthesis, particularly in the construction of complex molecules. The tert-butoxycarbonyl (Boc) group provides stability during reactions, allowing selective deprotection when needed. It is often employed in the development of pharmaceuticals, where precise control over molecular structure is critical. Additionally, it can be utilized in the preparation of drug candidates targeting neurological or metabolic disorders, owing to its ability to introduce specific functional groups into a molecule. Its tetrahydropyran ring structure also contributes to its use in creating compounds with enhanced bioavailability and stability.
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