(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-8-azido-2-methyloctanoic acid
98%
- Product Code: 232324
CAS:
1191429-14-7
| Molecular Weight: | 436.50 g./mol | Molecular Formula: | C₂₄H₂₈N₄O₄ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in peptide synthesis and bioconjugation processes, this compound serves as a protected chiral building block with a reactive azide group. The azide allows for click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient attachment of peptides to labels, polymers, or solid supports. The Fmoc group provides orthogonal protection for the amine, allowing stepwise assembly in solid-phase peptide synthesis. Its branched methyl group and extended chain offer steric and structural control, making it useful in designing peptidomimetics or probes for biochemical studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1mg | 10-20 days | ฿60,360.00 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-8-azido-2-methyloctanoic acid
Used in peptide synthesis and bioconjugation processes, this compound serves as a protected chiral building block with a reactive azide group. The azide allows for click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient attachment of peptides to labels, polymers, or solid supports. The Fmoc group provides orthogonal protection for the amine, allowing stepwise assembly in solid-phase peptide synthesis. Its branched methyl group and extended chain offer steric and structural control, making it useful in designing peptidomimetics or probes for biochemical studies.
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