2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(thiophen-2-yl)acetic acid
95%
- Product Code: 191348
CAS:
211682-11-0
| Molecular Weight: | 379.435 g./mol | Molecular Formula: | C₂₁H₁₇NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08458753 | |
| Melting Point: | Boiling Point: | 617.9±55.0 °C(Predicted) | |
| Density: | 1.370±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry, light-proof |
Product Description:
Widely used in peptide synthesis, this compound serves as a key building block for introducing thiophene-containing amino acid derivatives into peptide chains. Its main application lies in the preparation of modified peptides and peptidomimetics, where the thiophene ring can enhance metabolic stability or influence conformational behavior. The Fmoc group allows for mild, base-labile protection of the amine during solid-phase synthesis, making it compatible with standard Fmoc/tBu strategies. It is particularly valuable in the development of bioactive molecules, including pharmaceuticals and functional materials, where aromatic heterocycles like thiophene contribute to electronic or structural properties. Additionally, it has been employed in the synthesis of conjugated systems for use in organic electronics and fluorescent probes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿8,570.00 |
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| 0.250 G | 10-20 days | ฿14,550.00 |
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| 1.000 G | 10-20 days | ฿39,290.00 |
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2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(thiophen-2-yl)acetic acid
Widely used in peptide synthesis, this compound serves as a key building block for introducing thiophene-containing amino acid derivatives into peptide chains. Its main application lies in the preparation of modified peptides and peptidomimetics, where the thiophene ring can enhance metabolic stability or influence conformational behavior. The Fmoc group allows for mild, base-labile protection of the amine during solid-phase synthesis, making it compatible with standard Fmoc/tBu strategies. It is particularly valuable in the development of bioactive molecules, including pharmaceuticals and functional materials, where aromatic heterocycles like thiophene contribute to electronic or structural properties. Additionally, it has been employed in the synthesis of conjugated systems for use in organic electronics and fluorescent probes.
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