(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidine-3-carboxylic acid
98%
- Product Code: 37956
CAS:
193693-68-4
| Molecular Weight: | 351.40 g./mol | Molecular Formula: | C₂₁H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04112682 | |
| Melting Point: | Boiling Point: | 561.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is widely used in peptide synthesis as a protecting group for amines. Its fluorenylmethoxycarbonyl (Fmoc) group is particularly valuable in solid-phase peptide synthesis, where it protects the amine functionality during the coupling of amino acids. The Fmoc group can be easily removed under mild basic conditions, making it a preferred choice for constructing complex peptides. Additionally, its piperidine-3-carboxylic acid structure contributes to its stability and compatibility with various organic solvents, ensuring efficient and selective reactions in peptide chain assembly.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft7,660.39 |
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| 1.000 | 10-20 days | Ft19,393.39 |
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| 5.000 | 10-20 days | Ft68,361.72 |
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| 10.000 | 10-20 days | Ft135,753.76 |
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(S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidine-3-carboxylic acid
This chemical is widely used in peptide synthesis as a protecting group for amines. Its fluorenylmethoxycarbonyl (Fmoc) group is particularly valuable in solid-phase peptide synthesis, where it protects the amine functionality during the coupling of amino acids. The Fmoc group can be easily removed under mild basic conditions, making it a preferred choice for constructing complex peptides. Additionally, its piperidine-3-carboxylic acid structure contributes to its stability and compatibility with various organic solvents, ensuring efficient and selective reactions in peptide chain assembly.
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