(R)-3-(((Benzyloxy)carbonyl)amino)-4,4-dimethylpentanoic acid
97%
- Product Code: 56017
CAS:
872423-95-5
| Molecular Weight: | 279.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD18711403 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs, particularly in the synthesis of complex molecules with specific chiral centers. Its structure, featuring a benzyloxycarbonyl protecting group, makes it valuable in protecting amino groups during peptide coupling reactions, ensuring selective and efficient synthesis. Additionally, it is employed in the preparation of biologically active compounds, including enzyme inhibitors and receptor modulators, due to its ability to introduce specific stereochemistry and functional groups into target molecules. Its applications also extend to medicinal chemistry, where it contributes to the design and optimization of drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,662.00 |
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| 0.250 | 10-20 days | ฿9,333.00 |
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(R)-3-(((Benzyloxy)carbonyl)amino)-4,4-dimethylpentanoic acid
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of peptide-based drugs, particularly in the synthesis of complex molecules with specific chiral centers. Its structure, featuring a benzyloxycarbonyl protecting group, makes it valuable in protecting amino groups during peptide coupling reactions, ensuring selective and efficient synthesis. Additionally, it is employed in the preparation of biologically active compounds, including enzyme inhibitors and receptor modulators, due to its ability to introduce specific stereochemistry and functional groups into target molecules. Its applications also extend to medicinal chemistry, where it contributes to the design and optimization of drug candidates with improved efficacy and selectivity.
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