(S)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid
97%
- Product Code: 38111
CAS:
193693-62-8
| Molecular Weight: | 365.42 g./mol | Molecular Formula: | C₂₂H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656476 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amines. The fluorenylmethoxycarbonyl (Fmoc) group, a key component, is widely employed in solid-phase peptide synthesis to protect the amino group of amino acids. It allows for the sequential addition of amino acids to build peptides, as the Fmoc group can be easily removed under mild basic conditions without affecting other functional groups. Additionally, the piperidine ring in the structure can contribute to the conformational stability of the peptide chain, making it valuable in the development of bioactive peptides and pharmaceutical compounds. Its application extends to the synthesis of complex organic molecules and drug intermediates, where selective protection and deprotection strategies are essential.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,716.00 |
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| 0.250 | 10-20 days | ฿9,432.00 |
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(S)-2-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)piperidin-2-yl)acetic acid
This chemical is primarily used in peptide synthesis as a protecting group for amines. The fluorenylmethoxycarbonyl (Fmoc) group, a key component, is widely employed in solid-phase peptide synthesis to protect the amino group of amino acids. It allows for the sequential addition of amino acids to build peptides, as the Fmoc group can be easily removed under mild basic conditions without affecting other functional groups. Additionally, the piperidine ring in the structure can contribute to the conformational stability of the peptide chain, making it valuable in the development of bioactive peptides and pharmaceutical compounds. Its application extends to the synthesis of complex organic molecules and drug intermediates, where selective protection and deprotection strategies are essential.
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