Fmoc-D-Tyr(4-Et)-OH

97%

Reagent Code: #67473
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CAS Number 162502-65-0

science Other reagents with same CAS 162502-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 431.48 g/mol
Formula C₂₆H₂₅NO₅
thermostat Physical Properties
Boiling Point 654.3±55.0°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a building block for incorporating modified tyrosine residues into peptides. The Fmoc group protects the amino group during synthesis, while the ethyl modification on the tyrosine side chain can influence the peptide's properties, such as hydrophobicity or binding affinity. It is valuable in creating peptides for research in biochemistry, drug development, and molecular biology, especially where specific tyrosine modifications are required for functional studies or therapeutic applications.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,100.00
250mg
10-20 days ฿420.00
5g
10-20 days ฿3,480.00
25g
10-20 days ฿13,360.00
Fmoc-D-Tyr(4-Et)-OH
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Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a building block for incorporating modified tyrosine residues into peptides. The Fmoc group protects the amino group during synthesis, while the ethyl modification on the tyrosine side chain can influence the peptide's properties, such as hydrophobicity or binding affinity. It is valuable in creating peptides for research in biochemistry, drug development, and molecular biology, especially where specific tyrosine modifica

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a building block for incorporating modified tyrosine residues into peptides. The Fmoc group protects the amino group during synthesis, while the ethyl modification on the tyrosine side chain can influence the peptide's properties, such as hydrophobicity or binding affinity. It is valuable in creating peptides for research in biochemistry, drug development, and molecular biology, especially where specific tyrosine modifications are required for functional studies or therapeutic applications.

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