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

98%

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

science Other reagents with same CAS 672917-68-9

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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿5,750.00
250mg
10-20 days ฿9,540.00
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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