H-Phe(3-Br)-OH

97%

Reagent Code: #97466
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CAS Number 82311-69-1

science Other reagents with same CAS 82311-69-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.09 g/mol
Formula C₉H₁₀BrNO₂
badge Registry Numbers
MDL Number MFCD06659110
thermostat Physical Properties
Melting Point 218.0-218.2°C
Boiling Point 368.4°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily used in peptide synthesis as a building block for creating modified peptides. Its bromine substitution on the phenylalanine side chain allows for selective chemical modifications, making it valuable in designing peptide-based drugs or bioactive molecules. It is often employed in research to study enzyme-substrate interactions, receptor binding, or to introduce halogenated motifs into peptides for enhanced stability or activity. Additionally, it serves as a key intermediate in the development of pharmaceuticals targeting specific biological pathways, particularly in cases where halogenation can improve drug efficacy or pharmacokinetics.

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Test Parameter Specification
APPEARANCE White to off-white Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿270.00
inventory 5g
10-20 days ฿1,143.00

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H-Phe(3-Br)-OH
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This compound is primarily used in peptide synthesis as a building block for creating modified peptides. Its bromine substitution on the phenylalanine side chain allows for selective chemical modifications, making it valuable in designing peptide-based drugs or bioactive molecules. It is often employed in research to study enzyme-substrate interactions, receptor binding, or to introduce halogenated motifs into peptides for enhanced stability or activity. Additionally, it serves as a key intermediate in t

This compound is primarily used in peptide synthesis as a building block for creating modified peptides. Its bromine substitution on the phenylalanine side chain allows for selective chemical modifications, making it valuable in designing peptide-based drugs or bioactive molecules. It is often employed in research to study enzyme-substrate interactions, receptor binding, or to introduce halogenated motifs into peptides for enhanced stability or activity. Additionally, it serves as a key intermediate in the development of pharmaceuticals targeting specific biological pathways, particularly in cases where halogenation can improve drug efficacy or pharmacokinetics.

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