Fmoc-D-Phg-OH
98%
- Product Code: 66182
CAS:
111524-95-9
| Molecular Weight: | 373.4 g./mol | Molecular Formula: | C₂₃H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00190891 | |
| Melting Point: | 175-180°C | Boiling Point: | 606.3ºC at 760 mmHg |
| Density: | 1.299 g/cm3 | Storage Condition: | 2~8°C |
Product Description:
Fmoc-D-Phg-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of phenylglycine (Phg) introduces chirality, which is crucial for creating peptides with specific stereochemical properties. This compound is especially valuable in the synthesis of bioactive peptides, peptidomimetics, and other complex molecules used in drug discovery and biochemical research. Its stability and compatibility with standard SPPS protocols make it a reliable choice for peptide chemists.
Product Specification:
| Test | Specification |
|---|---|
| PURITYHPLC | 98 100% |
| MP | 175 180? |
| APPEARANCE | White crystal |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿290.00 |
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| 5.000 | 10-20 days | ฿680.00 |
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| 25.000 | 10-20 days | ฿2,400.00 |
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| 100.000 | 10-20 days | ฿8,250.00 |
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Fmoc-D-Phg-OH
Fmoc-D-Phg-OH is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the Fmoc (9-fluorenylmethoxycarbonyl) group acts as a temporary protecting group for the amine functionality. This allows for the sequential addition of amino acids to build peptides with high precision. The D-configuration of phenylglycine (Phg) introduces chirality, which is crucial for creating peptides with specific stereochemical properties. This compound is especially valuable in the synthesis of bioactive peptides, peptidomimetics, and other complex molecules used in drug discovery and biochemical research. Its stability and compatibility with standard SPPS protocols make it a reliable choice for peptide chemists.
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