Methyl 2-((tert-butoxycarbonyl)amino)pent-4-ynoate
95%
- Product Code: 213062
CAS:
173306-82-6
| Molecular Weight: | 227.26 g./mol | Molecular Formula: | C₁₁H₁₇NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656753 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key intermediate in peptide synthesis and organic chemistry, particularly in the preparation of modified amino acids and bioactive molecules. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation for drug discovery, bioconjugation, and the development of pharmaceutical compounds. The tert-butoxycarbonyl (Boc) protecting group ensures selective amine protection during multi-step syntheses, while the ester moiety can be hydrolyzed or further derivatized. Commonly employed in the construction of complex molecules where controlled reactivity and functional group compatibility are essential.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,700.00 |
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| 250mg | 10-20 days | ฿9,670.00 |
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| 1g | 10-20 days | ฿32,010.00 |
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Methyl 2-((tert-butoxycarbonyl)amino)pent-4-ynoate
Used as a key intermediate in peptide synthesis and organic chemistry, particularly in the preparation of modified amino acids and bioactive molecules. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation for drug discovery, bioconjugation, and the development of pharmaceutical compounds. The tert-butoxycarbonyl (Boc) protecting group ensures selective amine protection during multi-step syntheses, while the ester moiety can be hydrolyzed or further derivatized. Commonly employed in the construction of complex molecules where controlled reactivity and functional group compatibility are essential.
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