Fmoc-D-Phe(3-I)-OH

97%

Reagent Code: #50477
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CAS Number 478183-67-4

science Other reagents with same CAS 478183-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 513.32 g/mol
Formula C₂₄H₂₀INO₄
badge Registry Numbers
MDL Number MFCD03840402
thermostat Physical Properties
Boiling Point 658.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a building block for incorporating modified phenylalanine residues into peptides. The Fmoc group provides protection for the amino group during the synthesis process, while the iodine atom on the phenyl ring allows for further functionalization through cross-coupling reactions. This compound is valuable in the development of peptide-based drugs, biomaterials, and research tools, enabling the creation of peptides with specific structural and functional properties. Its application is especially relevant in medicinal chemistry and biochemistry for designing peptides with enhanced stability, binding affinity, or biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿37,836.00
250mg
10-20 days ฿2,286.00
1g
10-20 days ฿5,706.00
5g
10-20 days ฿23,040.00
Fmoc-D-Phe(3-I)-OH
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Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a building block for incorporating modified phenylalanine residues into peptides. The Fmoc group provides protection for the amino group during the synthesis process, while the iodine atom on the phenyl ring allows for further functionalization through cross-coupling reactions. This compound is valuable in the development of peptide-based drugs, biomaterials, and research tools, enabling the creation of peptides with spec

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a building block for incorporating modified phenylalanine residues into peptides. The Fmoc group provides protection for the amino group during the synthesis process, while the iodine atom on the phenyl ring allows for further functionalization through cross-coupling reactions. This compound is valuable in the development of peptide-based drugs, biomaterials, and research tools, enabling the creation of peptides with specific structural and functional properties. Its application is especially relevant in medicinal chemistry and biochemistry for designing peptides with enhanced stability, binding affinity, or biological activity.

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