(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tetrahydropyran-4-yl-propanoic acid
97%
- Product Code: 228728
CAS:
1879080-16-6
Molecular Weight: | 395.4483 g./mol | Molecular Formula: | C₂₃H₂₅NO₅ |
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EC Number: | MDL Number: | MFCD32640728 | |
Melting Point: | Boiling Point: | 626.4±35.0 °C(Predicted) | |
Density: | 1.250±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Widely used in peptide synthesis as a protected amino acid building block. The fluorenylmethoxycarbonyl (Fmoc) group enables reversible protection of the amine function, allowing stepwise assembly of peptides under mild basic conditions. The tetrahydropyran ring introduces conformational constraint, making this derivative valuable in the design of structurally defined peptides and peptidomimetics. Commonly employed in solid-phase peptide synthesis (SPPS) for producing pharmaceuticals, biochemical probes, and research compounds where stereochemical control and side-chain stability are critical. Its solubility in common organic solvents facilitates high coupling efficiency and purification.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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100mg | 10-20 days | €321.94 |
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500mg | 10-20 days | €1,071.81 |
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(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tetrahydropyran-4-yl-propanoic acid
Widely used in peptide synthesis as a protected amino acid building block. The fluorenylmethoxycarbonyl (Fmoc) group enables reversible protection of the amine function, allowing stepwise assembly of peptides under mild basic conditions. The tetrahydropyran ring introduces conformational constraint, making this derivative valuable in the design of structurally defined peptides and peptidomimetics. Commonly employed in solid-phase peptide synthesis (SPPS) for producing pharmaceuticals, biochemical probes, and research compounds where stereochemical control and side-chain stability are critical. Its solubility in common organic solvents facilitates high coupling efficiency and purification.
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