3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-nitrophenyl)propanoic acid
95%
- Product Code: 117348
CAS:
171778-06-6
| Molecular Weight: | 432.43 g./mol | Molecular Formula: | C₂₄H₂₀N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863202 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. The 2-nitrophenyl moiety can serve as a photolabile protecting group, allowing for selective deprotection under light exposure. This dual functionality makes it valuable in solid-phase peptide synthesis, where controlled deprotection and coupling steps are essential. Additionally, its structure enables efficient purification and isolation of peptides, ensuring high yields and purity in the final product.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,332.00 |
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| 0.250 | 10-20 days | ฿1,692.00 |
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| 1.000 | 10-20 days | ฿5,292.00 |
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| 5.000 | 10-20 days | ฿16,947.00 |
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3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(2-nitrophenyl)propanoic acid
This compound is primarily utilized in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. The 2-nitrophenyl moiety can serve as a photolabile protecting group, allowing for selective deprotection under light exposure. This dual functionality makes it valuable in solid-phase peptide synthesis, where controlled deprotection and coupling steps are essential. Additionally, its structure enables efficient purification and isolation of peptides, ensuring high yields and purity in the final product.
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