(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tetrahydropyran-4-yl-propanoic acid

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Reagent Code: #228728
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CAS Number 1879080-16-6

science Other reagents with same CAS 1879080-16-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 395.4483 g/mol
Formula C₂₃H₂₅NO₅
badge Registry Numbers
MDL Number MFCD32640728
thermostat Physical Properties
Boiling Point 626.4±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.250±0.06 g/cm3(Predicted)
Storage 2-8°C

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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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,240.00
inventory 500mg
10-20 days ฿40,750.00

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(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tetrahydropyran-4-yl-propanoic acid
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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,

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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