(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid

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Reagent Code: #236578
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CAS Number 1310680-44-4

science Other reagents with same CAS 1310680-44-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 440.49 g/mol
Formula C₂₄H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD08457841
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group allows for orthogonal protection of the alpha-amino group, enabling stepwise assembly of peptides with mild base-labile deprotection. The tert-butoxycarbonyl (Boc) group protects the side-chain amine, making it suitable for incorporating asparagine or aspartic acid derivatives selectively. Its stereochemistry ensures chiral purity in the resulting peptide chain. Commonly employed in the preparation of complex peptides and proteins for pharmaceutical and biochemical research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,920.00
inventory 250mg
10-20 days ฿10,340.00
inventory 1g
10-20 days ฿25,820.00

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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid
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Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group allows for orthogonal protection of the alpha-amino group, enabling stepwise assembly of peptides with mild base-labile deprotection. The tert-butoxycarbonyl (Boc) group protects the side-chain amine, making it suitable for incorporating asparagine or aspartic acid derivatives selectively. Its stereochemistry ensures chiral purity in the resulting peptide chain. Commonl

Used in peptide synthesis as a protected amino acid building block, particularly in solid-phase peptide synthesis (SPPS). The Fmoc group allows for orthogonal protection of the alpha-amino group, enabling stepwise assembly of peptides with mild base-labile deprotection. The tert-butoxycarbonyl (Boc) group protects the side-chain amine, making it suitable for incorporating asparagine or aspartic acid derivatives selectively. Its stereochemistry ensures chiral purity in the resulting peptide chain. Commonly employed in the preparation of complex peptides and proteins for pharmaceutical and biochemical research.

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