(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tetrahydropyran-4-yl-propanoic acid
97%
science Other reagents with same CAS 1879080-16-6
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description 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.
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