(R)-2-(((tert-Butoxycarbonyl)amino)methyl)-3-methylbutanoic acid
97%
- Product Code: 53050
CAS:
191664-14-9
| Molecular Weight: | 231.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD07372880 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in the synthesis of peptides and pharmaceuticals, serving as a key intermediate. It is particularly valuable in the preparation of chiral compounds due to its stereochemistry, which helps in creating enantiomerically pure substances. Its tert-butoxycarbonyl (Boc) protecting group is widely employed in peptide synthesis to shield the amino group during reactions, ensuring selective modifications. Additionally, it finds application in the development of bioactive molecules and drug candidates, especially in research focused on amino acid derivatives. Its structural features make it suitable for constructing complex organic molecules in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,720.00 |
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| 0.250 | 10-20 days | ฿15,390.00 |
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| 1.000 | 10-20 days | ฿44,550.00 |
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(R)-2-(((tert-Butoxycarbonyl)amino)methyl)-3-methylbutanoic acid
This chemical is primarily used in the synthesis of peptides and pharmaceuticals, serving as a key intermediate. It is particularly valuable in the preparation of chiral compounds due to its stereochemistry, which helps in creating enantiomerically pure substances. Its tert-butoxycarbonyl (Boc) protecting group is widely employed in peptide synthesis to shield the amino group during reactions, ensuring selective modifications. Additionally, it finds application in the development of bioactive molecules and drug candidates, especially in research focused on amino acid derivatives. Its structural features make it suitable for constructing complex organic molecules in medicinal chemistry.
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