(2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-methylpyrrolidine-2-carboxylic acid

95%

Reagent Code: #237500
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CAS Number 1228577-03-4

science Other reagents with same CAS 1228577-03-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.40 g/mol
Formula C₂₁H₂₁NO₄
badge Registry Numbers
MDL Number MFCD31716148
thermostat Physical Properties
Boiling Point 548.8±43.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.282±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected pyrrolidine derivative that enables stereoselective construction of complex molecules. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The methyl-substituted pyrrolidine core introduces conformational constraints, which are valuable in designing peptidomimetics and bioactive compounds with improved metabolic stability and receptor selectivity. Commonly employed in pharmaceutical research, especially in the development of protease inhibitors and central nervous system agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,260.00
inventory 250mg
10-20 days ฿10,610.00
inventory 1g
10-20 days ฿30,100.00
(2S,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-methylpyrrolidine-2-carboxylic acid
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Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected pyrrolidine derivative that enables stereoselective construction of complex molecules. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The methyl-substituted pyrrolidine core introduces conformational constraints, which are valuable in designing peptidomimetics and bioactive compounds with improved metabolic stability and receptor selec

Used primarily in peptide synthesis as a chiral building block, this compound serves as a protected pyrrolidine derivative that enables stereoselective construction of complex molecules. Its Fmoc group allows for mild base-labile protection, making it compatible with solid-phase peptide synthesis (SPPS). The methyl-substituted pyrrolidine core introduces conformational constraints, which are valuable in designing peptidomimetics and bioactive compounds with improved metabolic stability and receptor selectivity. Commonly employed in pharmaceutical research, especially in the development of protease inhibitors and central nervous system agents.

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