(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-methoxy-4-oxobutanoic acid
97%
- Product Code: 104320
CAS:
2044710-58-7
| Molecular Weight: | 383.39 g./mol | Molecular Formula: | C₂₁H₂₁NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30475935 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amine group during the synthesis process, ensuring that reactions occur at the desired sites without interference. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it highly useful in solid-phase peptide synthesis, where it allows for the stepwise construction of peptides with high precision. Additionally, the methoxy group in the structure can enhance solubility in organic solvents, facilitating smoother reactions in synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft34,617.21 |
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| 0.250 | 10-20 days | Ft40,726.13 |
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| 1.000 | 10-20 days | Ft115,390.70 |
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-methoxy-4-oxobutanoic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It helps in the selective protection of the amine group during the synthesis process, ensuring that reactions occur at the desired sites without interference. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of this compound, is particularly valued for its stability under basic conditions and its ease of removal under mild acidic conditions. This makes it highly useful in solid-phase peptide synthesis, where it allows for the stepwise construction of peptides with high precision. Additionally, the methoxy group in the structure can enhance solubility in organic solvents, facilitating smoother reactions in synthetic processes.
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