Fmoc-S-3-amino-4-(4-methoxyphenyl)-butyric acid

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Reagent Code: #105148
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CAS Number 1352435-52-9

science Other reagents with same CAS 1352435-52-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.48 g/mol
Formula C₂₆H₂₅NO₅
badge Registry Numbers
MDL Number MFCD22887414
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The presence of the 4-methoxyphenyl group in its structure makes it valuable for introducing specific aromatic and hydrophobic properties into peptide sequences, which can be crucial for studying peptide-protein interactions or designing bioactive peptides. Its application is prominent in pharmaceutical research, where it aids in the development of peptide-based drugs, enzyme inhibitors, and probes for biochemical studies. Additionally, it is utilized in the synthesis of modified peptides for exploring structure-activity relationships (SAR) in drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,007.00
inventory 5g
10-20 days ฿34,677.00
inventory 250mg
10-20 days ฿3,420.00
inventory 1g
10-20 days ฿7,227.00

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Fmoc-S-3-amino-4-(4-methoxyphenyl)-butyric acid
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This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a protected amino acid derivative, where the Fmoc (fluorenylmethyloxycarbonyl) group acts as a temporary protecting group for the amine functionality during the synthesis process. The presence of the 4-methoxyphenyl group in its structure makes it valuable for introducing specific aromatic and hydrophobic properties into peptide sequences, which can be crucial for studying peptide-protein interactions or designing bioactive peptides. Its application is prominent in pharmaceutical research, where it aids in the development of peptide-based drugs, enzyme inhibitors, and probes for biochemical studies. Additionally, it is utilized in the synthesis of modified peptides for exploring structure-activity relationships (SAR) in drug discovery.
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