3-((tert-Butoxycarbonyl)amino)-2-hydroxypropanoic acid
97%
- Product Code: 50424
CAS:
218916-64-4
| Molecular Weight: | 205.21 g./mol | Molecular Formula: | C₈H₁₅NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275906 | |
| Melting Point: | Boiling Point: | 391.742°C at 760 mmHg | |
| Density: | 1.24g/cm3 | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a protected form of amino acid, where the tert-butoxycarbonyl (Boc) group shields the amino functionality during chemical reactions, allowing selective modification of other parts of the molecule. This protection is crucial in peptide synthesis to prevent unwanted side reactions and ensure the correct sequence of amino acids. Additionally, it is utilized in the development of pharmaceuticals, where its hydroxyl and carboxyl groups can be further functionalized to create drug intermediates or active ingredients. Its stability and ease of deprotection make it a valuable building block in medicinal chemistry and biochemical research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $115.38 |
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| 1.000 | 10-20 days | $289.52 |
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| 5.000 | 10-20 days | $873.86 |
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| 10.000 | 10-20 days | $1,458.21 |
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3-((tert-Butoxycarbonyl)amino)-2-hydroxypropanoic acid
This chemical is primarily used in organic synthesis, particularly in the preparation of peptides and other biologically active compounds. It serves as a protected form of amino acid, where the tert-butoxycarbonyl (Boc) group shields the amino functionality during chemical reactions, allowing selective modification of other parts of the molecule. This protection is crucial in peptide synthesis to prevent unwanted side reactions and ensure the correct sequence of amino acids. Additionally, it is utilized in the development of pharmaceuticals, where its hydroxyl and carboxyl groups can be further functionalized to create drug intermediates or active ingredients. Its stability and ease of deprotection make it a valuable building block in medicinal chemistry and biochemical research.
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