N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-benzyl-L-alanine

98%

Reagent Code: #220576
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CAS Number 672917-68-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 401.45 g/mol
Formula C₂₅H₂₃NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in peptide synthesis as a protected amino acid building block. The Fmoc group provides temporary protection for the amine functionality, allowing selective coupling reactions in solid-phase and solution-phase peptide assembly. The N-benzyl group enhances solubility in organic solvents and offers stability during deprotection steps, compatible with Fmoc-strategy workflows. Enables the synthesis of complex peptides with reduced side reactions. Commonly employed in the preparation of pharmaceutical intermediates, bioactive peptides, and research compounds requiring precise sequence control.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,750.00
inventory 250mg
10-20 days ฿9,540.00
inventory 1g
10-20 days ฿27,920.00
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-benzyl-L-alanine
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Widely used in peptide synthesis as a protected amino acid building block. The Fmoc group provides temporary protection for the amine functionality, allowing selective coupling reactions in solid-phase and solution-phase peptide assembly. The N-benzyl group enhances solubility in organic solvents and offers stability during deprotection steps, compatible with Fmoc-strategy workflows. Enables the synthesis of complex peptides with reduced side reactions. Commonly employed in the preparation of pharmaceutical
Widely used in peptide synthesis as a protected amino acid building block. The Fmoc group provides temporary protection for the amine functionality, allowing selective coupling reactions in solid-phase and solution-phase peptide assembly. The N-benzyl group enhances solubility in organic solvents and offers stability during deprotection steps, compatible with Fmoc-strategy workflows. Enables the synthesis of complex peptides with reduced side reactions. Commonly employed in the preparation of pharmaceutical intermediates, bioactive peptides, and research compounds requiring precise sequence control.
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