2-(Tert-Butoxycarbonylamino)-4-Methoxy-4-Oxobutanoic Acid
97%
- Product Code: 241145
CAS:
856417-64-6
| Molecular Weight: | 247.25 g./mol | Molecular Formula: | C₁₀H₁₇NO₆ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used primarily as a protected amino acid derivative in peptide synthesis. The Boc (tert-butoxycarbonyl) group acts as a protecting group for the amine functionality, allowing selective reaction at the carboxylic acid end. The methyl ester at the other end can be selectively hydrolyzed or used in coupling reactions. Commonly employed in solid-phase and solution-phase peptide synthesis to build complex protein fragments. Its stability under a range of reaction conditions makes it valuable in multi-step organic syntheses, particularly in pharmaceutical development where controlled assembly of amino acid sequences is required. Also used in the preparation of enzyme inhibitors and bioactive molecules.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿1,730.00 |
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| 5.000 G | 10-20 days | ฿7,920.00 |
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| 10.000 G | 10-20 days | ฿13,730.00 |
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| 25.000 G | 10-20 days | ฿28,200.00 |
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2-(Tert-Butoxycarbonylamino)-4-Methoxy-4-Oxobutanoic Acid
Used primarily as a protected amino acid derivative in peptide synthesis. The Boc (tert-butoxycarbonyl) group acts as a protecting group for the amine functionality, allowing selective reaction at the carboxylic acid end. The methyl ester at the other end can be selectively hydrolyzed or used in coupling reactions. Commonly employed in solid-phase and solution-phase peptide synthesis to build complex protein fragments. Its stability under a range of reaction conditions makes it valuable in multi-step organic syntheses, particularly in pharmaceutical development where controlled assembly of amino acid sequences is required. Also used in the preparation of enzyme inhibitors and bioactive molecules.
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