2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)-2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamido)acetic acid
95%
- Product Code: 215713
CAS:
959151-70-3
| Molecular Weight: | 492.48 g./mol | Molecular Formula: | C₂₅H₂₄N₄O₇ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in peptide synthesis, this compound serves as a key building block for incorporating modified amino acids into peptide chains. Its structure allows for selective protection and deprotection during solid-phase synthesis, making it valuable in the development of complex peptides with precise sequences. The presence of the fluorenylmethyloxycarbonyl (Fmoc) group enables mild base-labile protection, compatible with Fmoc-strategy workflows. It is particularly useful in the preparation of bioactive peptides, peptide conjugates, and peptidomimetics for pharmaceutical research. Additionally, its functional handles support conjugation to labels, tags, or solid supports, facilitating applications in drug discovery, diagnostics, and biochemical assays.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,560.00 |
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| 0.250 | 10-20 days | ฿6,010.00 |
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| 1.000 | 10-20 days | ฿16,200.00 |
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2-(N-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethyl)-2-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamido)acetic acid
Widely used in peptide synthesis, this compound serves as a key building block for incorporating modified amino acids into peptide chains. Its structure allows for selective protection and deprotection during solid-phase synthesis, making it valuable in the development of complex peptides with precise sequences. The presence of the fluorenylmethyloxycarbonyl (Fmoc) group enables mild base-labile protection, compatible with Fmoc-strategy workflows. It is particularly useful in the preparation of bioactive peptides, peptide conjugates, and peptidomimetics for pharmaceutical research. Additionally, its functional handles support conjugation to labels, tags, or solid supports, facilitating applications in drug discovery, diagnostics, and biochemical assays.
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