2-(((((9H-fluorene-9-yl) methoxy) carbonyl) (2,4-dimethoxybenzyl) amino) acetic acid
97%
- Product Code: 41090
CAS:
166881-42-1
| Molecular Weight: | 447.48 g./mol | Molecular Formula: | C₂₆H₂₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08064316 | |
| Melting Point: | Boiling Point: | 653.2 °C at 760 mmHg | |
| Density: | 1.280±0.06 g/cm3 | Storage Condition: | 2-8℃, inert gas |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amino acids during the synthesis of peptides. The fluorenylmethoxycarbonyl (Fmoc) group, a component of this compound, is widely used due to its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision and yield. Additionally, the 2,4-dimethoxybenzyl group provides further protection for specific functional groups, enhancing the selectivity and efficiency of the synthesis process. Its application is critical in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies.
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 |
|---|---|---|---|
| 0.250 | 10-20 days | £65.14 |
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| 1.000 | 10-20 days | £151.76 |
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| 5.000 | 10-20 days | £535.57 |
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2-(((((9H-fluorene-9-yl) methoxy) carbonyl) (2,4-dimethoxybenzyl) amino) acetic acid
This chemical is primarily utilized in the field of organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amino acids during the synthesis of peptides. The fluorenylmethoxycarbonyl (Fmoc) group, a component of this compound, is widely used due to its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis (SPPS), allowing for the stepwise construction of peptides with high precision and yield. Additionally, the 2,4-dimethoxybenzyl group provides further protection for specific functional groups, enhancing the selectivity and efficiency of the synthesis process. Its application is critical in the production of complex peptides for pharmaceutical research, drug development, and biochemical studies.
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