(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-2-phenylacetic acid

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Reagent Code: #38017
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CAS Number 574739-36-9

science Other reagents with same CAS 574739-36-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 387.43 g/mol
Formula C₂₄H₂₁NO₄
badge Registry Numbers
MDL Number MFCD01861296
thermostat Physical Properties
Boiling Point 580.4±39.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly when an N-methylated phenylglycine residue is required. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety on the amino group, preventing unwanted reactions during the peptide assembly process. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology. The compound's stability and ease of deprotection make it a valuable reagent in solid-phase peptide synthesis, enabling the production of high-purity peptides for therapeutic and experimental purposes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿972.00
inventory 5g
10-20 days ฿3,951.00
inventory 10g
10-20 days ฿6,426.00
inventory 250mg
10-20 days ฿387.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-2-phenylacetic acid
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This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly when an N-methylated phenylglycine residue is required. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety on the amino group, preventing unwanted reactions during the peptide assembly process. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools in

This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides with specific sequences, particularly when an N-methylated phenylglycine residue is required. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety on the amino group, preventing unwanted reactions during the peptide assembly process. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research tools in biochemistry and molecular biology. The compound's stability and ease of deprotection make it a valuable reagent in solid-phase peptide synthesis, enabling the production of high-purity peptides for therapeutic and experimental purposes.

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