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

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Reagent Code: #38020
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CAS Number 1640968-91-7

science Other reagents with same CAS 1640968-91-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.58 g/mol
Formula C₂₈H₃₅NO₄
badge Registry Numbers
MDL Number MFCD30471500
thermostat Physical Properties
Boiling Point 620.3±38.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, dry sealed

description Product Description

This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides. The Fmoc group can be selectively removed under mild basic conditions, ensuring the integrity of the peptide chain. Additionally, the presence of the methyldodec-11-enoic acid moiety may contribute to the compound's solubility and stability in organic solvents, facilitating its use in complex peptide synthesis workflows. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research in biochemistry and molecular biology.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,174.00
inventory 250mg
10-20 days ฿12,357.00

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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-methyldodec-11-enoic acid
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This compound is primarily used in peptide synthesis as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group shields the amino group during the synthesis process, preventing unwanted reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS), where it allows for the stepwise assembly of peptides. The Fmoc group can be selectively removed under mild basic conditions, ensuring the integrity of the peptide chain. Additionally, the presence of the methyldodec-11-enoic acid moiety may contribute to the compound's solubility and stability in organic solvents, facilitating its use in complex peptide synthesis workflows. Its application is crucial in the development of pharmaceuticals, bioactive peptides, and research in biochemistry and molecular biology.
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