4-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid

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Reagent Code: #39854
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CAS Number 218278-58-1

science Other reagents with same CAS 218278-58-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.5100 g/mol
Formula C₂₅H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD01076217
inventory_2 Storage & Handling
Storage -20°C

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as orthogonal protective groups for the two nitrogen atoms of the piperazine ring. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptides with high precision. The Fmoc group can be selectively removed under mild basic conditions, while the Boc group requires acidic conditions, allowing for controlled deprotection during synthesis. This compound is particularly valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿999.00

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4-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
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This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as orthogonal protective groups for the two nitrogen atoms of the piperazine ring. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptides with high precision. The Fmoc group can be selectively removed under m

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, where the fluorenylmethoxycarbonyl (Fmoc) and tert-butoxycarbonyl (Boc) groups act as orthogonal protective groups for the two nitrogen atoms of the piperazine ring. Its application is crucial in solid-phase peptide synthesis (SPPS), enabling the stepwise assembly of peptides with high precision. The Fmoc group can be selectively removed under mild basic conditions, while the Boc group requires acidic conditions, allowing for controlled deprotection during synthesis. This compound is particularly valuable in producing peptides for pharmaceutical research, drug development, and biochemical studies.

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