(2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-phenylpyrrolidine-2-carboxylic acid
≥95%
- Product Code: 36547
CAS:
1093651-96-7
| Molecular Weight: | 413.47 g./mol | Molecular Formula: | C₂₆H₂₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656464 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amine functionality during the synthesis process, preventing unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides on a resin. The Fmoc group can be easily removed under mild basic conditions, ensuring the integrity of the peptide chain. Additionally, its chiral structure makes it suitable for synthesizing stereospecific peptides, which are critical in pharmaceutical research and drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,720.00 |
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| 0.250 | 10-20 days | ฿15,498.00 |
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| 1.000 | 10-20 days | ฿38,817.00 |
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(2S,4R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-phenylpyrrolidine-2-carboxylic acid
This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amine functionality during the synthesis process, preventing unwanted side reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides on a resin. The Fmoc group can be easily removed under mild basic conditions, ensuring the integrity of the peptide chain. Additionally, its chiral structure makes it suitable for synthesizing stereospecific peptides, which are critical in pharmaceutical research and drug development.
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