3-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethoxy)propanoic acid
97%
- Product Code: 44218
CAS:
1654740-73-4
| Molecular Weight: | 355.38 g./mol | Molecular Formula: | C₂₀H₂₁NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16294357 | |
| Melting Point: | Boiling Point: | 589.9±40.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It is particularly effective in solid-phase peptide synthesis (SPPS), where it helps to protect the amino group during the coupling reactions. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of this compound, is stable under basic conditions but can be easily removed using piperidine, allowing for selective deprotection. This makes it a valuable tool in the stepwise construction of peptides, ensuring high yields and purity. Additionally, it is utilized in the synthesis of complex organic molecules where temporary protection of functional groups is required. Its compatibility with various solvents and reagents further enhances its versatility in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,680.00 |
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| 0.250 | 10-20 days | ฿3,360.00 |
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| 1.000 | 10-20 days | ฿5,560.00 |
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3-(2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)ethoxy)propanoic acid
This chemical is primarily used in peptide synthesis as a protecting group for amino acids. It is particularly effective in solid-phase peptide synthesis (SPPS), where it helps to protect the amino group during the coupling reactions. The fluorenylmethoxycarbonyl (Fmoc) group, which is part of this compound, is stable under basic conditions but can be easily removed using piperidine, allowing for selective deprotection. This makes it a valuable tool in the stepwise construction of peptides, ensuring high yields and purity. Additionally, it is utilized in the synthesis of complex organic molecules where temporary protection of functional groups is required. Its compatibility with various solvents and reagents further enhances its versatility in organic synthesis.
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