Fmoc-O-t-butyl-L-beta-homotyrosine

98%

Reagent Code: #59226
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CAS Number 219967-69-8

science Other reagents with same CAS 219967-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 473.57 g/mol
Formula C₂₉H₃₁NO₅
badge Registry Numbers
MDL Number MFCD01862862
thermostat Physical Properties
Melting Point 105-110℃
Boiling Point 671.4 °C at 760mmHg
inventory_2 Storage & Handling
Density 1.203 g/cm3
Storage 2-8°C

description Product Description

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a protected amino acid derivative. The Fmoc group provides protection for the amino group during the synthesis process, while the O-t-butyl group protects the hydroxyl group of the tyrosine side chain. This allows for selective deprotection and coupling steps, enabling the construction of complex peptide sequences. It is especially valuable in the synthesis of peptides containing beta-homotyrosine, a non-natural amino acid, which can be incorporated into peptides to study structure-activity relationships or to enhance peptide stability and bioavailability. This compound is also utilized in the development of peptide-based drugs, biomaterials, and research tools for studying protein interactions and functions.

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Test Parameter Specification
Appearance White to Off-white Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,665.00
inventory 250mg
10-20 days ฿2,781.00

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Fmoc-O-t-butyl-L-beta-homotyrosine
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Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a protected amino acid derivative. The Fmoc group provides protection for the amino group during the synthesis process, while the O-t-butyl group protects the hydroxyl group of the tyrosine side chain. This allows for selective deprotection and coupling steps, enabling the construction of complex peptide sequences. It is especially valuable in the synthesis of peptides containing beta-homotyrosine, a non-natural amino aci

Used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), as a protected amino acid derivative. The Fmoc group provides protection for the amino group during the synthesis process, while the O-t-butyl group protects the hydroxyl group of the tyrosine side chain. This allows for selective deprotection and coupling steps, enabling the construction of complex peptide sequences. It is especially valuable in the synthesis of peptides containing beta-homotyrosine, a non-natural amino acid, which can be incorporated into peptides to study structure-activity relationships or to enhance peptide stability and bioavailability. This compound is also utilized in the development of peptide-based drugs, biomaterials, and research tools for studying protein interactions and functions.

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