L-Glutamine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-phenyl-

98%

Reagent Code: #201637
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CAS Number 198134-12-2

science Other reagents with same CAS 198134-12-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 444.4792 g/mol
Formula C₂₆H₂₄N₂O₅
thermostat Physical Properties
Boiling Point 753.4±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.320±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a protected amino acid building block in solid-phase peptide synthesis (SPPS), this compound enables selective and efficient incorporation of glutamine residues into peptide chains. The fluorenylmethyloxycarbonyl (Fmoc) group protects the alpha-amino function, allowing for mild base-induced deprotection under piperidine treatment, while the N-phenyl group stabilizes the side chain amide. Its main application lies in the synthesis of complex peptides and proteins in research and pharmaceutical development, particularly where glutamine side-chain reactivity needs to be controlled. It is compatible with resin-bound synthesis and widely used in automated peptide synthesizers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,200.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿12,800.00

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L-Glutamine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-N-phenyl-
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Used primarily as a protected amino acid building block in solid-phase peptide synthesis (SPPS), this compound enables selective and efficient incorporation of glutamine residues into peptide chains. The fluorenylmethyloxycarbonyl (Fmoc) group protects the alpha-amino function, allowing for mild base-induced deprotection under piperidine treatment, while the N-phenyl group stabilizes the side chain amide. Its main application lies in the synthesis of complex peptides and proteins in research and pharmaceuti
Used primarily as a protected amino acid building block in solid-phase peptide synthesis (SPPS), this compound enables selective and efficient incorporation of glutamine residues into peptide chains. The fluorenylmethyloxycarbonyl (Fmoc) group protects the alpha-amino function, allowing for mild base-induced deprotection under piperidine treatment, while the N-phenyl group stabilizes the side chain amide. Its main application lies in the synthesis of complex peptides and proteins in research and pharmaceutical development, particularly where glutamine side-chain reactivity needs to be controlled. It is compatible with resin-bound synthesis and widely used in automated peptide synthesizers.
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