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

95%

Reagent Code: #230683
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CAS Number 1217723-28-8

science Other reagents with same CAS 1217723-28-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 452.50 g/mol
Formula C₂₅H₂₈N₂O₆
badge Registry Numbers
MDL Number MFCD02179100
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in peptide synthesis and medicinal chemistry as a chiral building block. Its main application lies in the preparation of complex organic molecules where stereochemical control is essential. The compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide synthesis. It is especially valuable in the development of pharmaceutical intermediates, including protease inhibitors and other bioactive compounds. The presence of orthogonal protecting groups (Fmoc and Boc) allows for stepwise deprotection and coupling, making it ideal for automated synthesis and the construction of multi-step molecular architectures.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,330.00
inventory 250mg
10-20 days ฿4,300.00
inventory 1g
10-20 days ฿16,660.00
inventory 5g
10-20 days ฿82,350.00
(R)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-(tert-butoxycarbonyl)piperazine-2-carboxylic acid
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Used primarily in peptide synthesis and medicinal chemistry as a chiral building block. Its main application lies in the preparation of complex organic molecules where stereochemical control is essential. The compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide synthesis. It is especially valuable in the development of pharmaceutical intermediates, including protease inhibitors and other bioactive compounds. The presence of

Used primarily in peptide synthesis and medicinal chemistry as a chiral building block. Its main application lies in the preparation of complex organic molecules where stereochemical control is essential. The compound serves as a protected amino acid derivative, enabling selective coupling reactions in solid-phase and solution-phase peptide synthesis. It is especially valuable in the development of pharmaceutical intermediates, including protease inhibitors and other bioactive compounds. The presence of orthogonal protecting groups (Fmoc and Boc) allows for stepwise deprotection and coupling, making it ideal for automated synthesis and the construction of multi-step molecular architectures.

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