(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldodec-11-enoic acid

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Reagent Code: #37416
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CAS Number 2061996-53-8

science Other reagents with same CAS 2061996-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.58 g/mol
Formula C₁₄H₁₁NO
badge Registry Numbers
MDL Number MFCD30573983
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily used in the field of peptide synthesis, where it serves as a building block for creating complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the selective deprotection and coupling of amino acids. The compound’s structure, including the long aliphatic chain and terminal double bond, makes it suitable for introducing hydrophobic or functionalized segments into peptides, which can be crucial for studying protein interactions or developing therapeutic agents. Additionally, its chiral center ensures the synthesis of enantiomerically pure peptides, which is essential for maintaining biological activity in pharmaceutical applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,671.00
inventory 250mg
10-20 days ฿9,342.00

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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldodec-11-enoic acid
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This chemical is primarily used in the field of peptide synthesis, where it serves as a building block for creating complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the selective deprotection and coupling of amino acids. The compound’s structure, including the long aliphatic chain and terminal double bond, makes it suitable for introducing hydrophobic or functionalized segments into peptides, which can

This chemical is primarily used in the field of peptide synthesis, where it serves as a building block for creating complex peptide structures. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly valuable in solid-phase peptide synthesis, allowing for the selective deprotection and coupling of amino acids. The compound’s structure, including the long aliphatic chain and terminal double bond, makes it suitable for introducing hydrophobic or functionalized segments into peptides, which can be crucial for studying protein interactions or developing therapeutic agents. Additionally, its chiral center ensures the synthesis of enantiomerically pure peptides, which is essential for maintaining biological activity in pharmaceutical applications.

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