(S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate

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Reagent Code: #37847
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CAS Number 146803-41-0

science Other reagents with same CAS 146803-41-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₈H₁₇NO₃
badge Registry Numbers
MDL Number MFCD01318541
thermostat Physical Properties
Boiling Point 479.9±28.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, store under inert gas

description Product Description

This compound, (S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate, is the Fmoc-protected derivative of L-alaninal. It serves as a key building block in advanced peptide synthesis, particularly for incorporating an aldehyde group at the C-terminus of peptides. The Fmoc protecting group safeguards the N-terminal amino function, enabling orthogonal deprotection and selective coupling in solid-phase or solution-phase methodologies. This reagent is essential for synthesizing peptide aldehydes used in native chemical ligation, protease inhibitor development, and bioactive molecule construction. Its stability and compatibility with standard synthesis protocols make it invaluable in biochemical research and medicinal chemistry for creating complex peptide-based therapeutics.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 96.5-100%
Mass Spectrum Conforms to Structure
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,593.00
inventory 250mg
10-20 days ฿5,301.00

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(S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate
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This compound, (S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate, is the Fmoc-protected derivative of L-alaninal. It serves as a key building block in advanced peptide synthesis, particularly for incorporating an aldehyde group at the C-terminus of peptides. The Fmoc protecting group safeguards the N-terminal amino function, enabling orthogonal deprotection and selective coupling in solid-phase or solution-phase methodologies. This reagent is essential for synthesizing peptide aldehydes used in nat

This compound, (S)-(9H-Fluoren-9-yl)methyl (1-oxopropan-2-yl)carbamate, is the Fmoc-protected derivative of L-alaninal. It serves as a key building block in advanced peptide synthesis, particularly for incorporating an aldehyde group at the C-terminus of peptides. The Fmoc protecting group safeguards the N-terminal amino function, enabling orthogonal deprotection and selective coupling in solid-phase or solution-phase methodologies. This reagent is essential for synthesizing peptide aldehydes used in native chemical ligation, protease inhibitor development, and bioactive molecule construction. Its stability and compatibility with standard synthesis protocols make it invaluable in biochemical research and medicinal chemistry for creating complex peptide-based therapeutics.

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