(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
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
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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