2-(((9H-Fluoren-9-yl)methoxy)carbonyl)isoindoline-1-carboxylic acid
95%
- Product Code: 41104
CAS:
204320-59-2
| Molecular Weight: | 385.41 g./mol | Molecular Formula: | C₂₄H₁₉NO₄ |
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| EC Number: | MDL Number: | MFCD00270204 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of the molecule, is widely employed in solid-phase peptide synthesis (SPPS) to protect the amino group of amino acids during the assembly of peptide chains. Its key advantage lies in its stability under the reaction conditions used for peptide bond formation, while being easily removable under mild basic conditions, typically using piperidine. This allows for the stepwise construction of peptides with high efficiency and precision. Additionally, the isoindoline moiety contributes to the stability and handling of the compound during chemical processes. Its application is critical in the production of peptides for pharmaceutical research, drug development, and biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $179.09 |
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2-(((9H-Fluoren-9-yl)methoxy)carbonyl)isoindoline-1-carboxylic acid
This chemical is primarily utilized in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of the molecule, is widely employed in solid-phase peptide synthesis (SPPS) to protect the amino group of amino acids during the assembly of peptide chains. Its key advantage lies in its stability under the reaction conditions used for peptide bond formation, while being easily removable under mild basic conditions, typically using piperidine. This allows for the stepwise construction of peptides with high efficiency and precision. Additionally, the isoindoline moiety contributes to the stability and handling of the compound during chemical processes. Its application is critical in the production of peptides for pharmaceutical research, drug development, and biochemical studies.
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