L-Tyrosine,N-[(1,1-dimethylethoxy)carbonyl]-O-ethyl-,methyl ester

98%

Reagent Code: #202754
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CAS Number 92507-32-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.38 g/mol
Formula C₁₇H₂₅NO₅
thermostat Physical Properties
Boiling Point 449.8±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.098±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

This protected L-tyrosine derivative, with N-(tert-butoxycarbonyl) (Boc) on the amino group, O-ethyl on the phenolic side chain, and methyl ester on the carboxylic acid, serves as a key intermediate in peptide synthesis for pharmaceuticals and bioactive peptides. The Boc group protects the amino terminus, allowing selective deprotection under mild acidic conditions, while the ester functionalities safeguard the side chain and C-terminus, facilitating precise stepwise assembly of complex peptide chains. It is widely used in solid-phase peptide synthesis and the development of enzyme inhibitors or receptor ligands.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,520.00
L-Tyrosine,N-[(1,1-dimethylethoxy)carbonyl]-O-ethyl-,methyl ester
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This protected L-tyrosine derivative, with N-(tert-butoxycarbonyl) (Boc) on the amino group, O-ethyl on the phenolic side chain, and methyl ester on the carboxylic acid, serves as a key intermediate in peptide synthesis for pharmaceuticals and bioactive peptides. The Boc group protects the amino terminus, allowing selective deprotection under mild acidic conditions, while the ester functionalities safeguard the side chain and C-terminus, facilitating precise stepwise assembly of complex peptide chains. I

This protected L-tyrosine derivative, with N-(tert-butoxycarbonyl) (Boc) on the amino group, O-ethyl on the phenolic side chain, and methyl ester on the carboxylic acid, serves as a key intermediate in peptide synthesis for pharmaceuticals and bioactive peptides. The Boc group protects the amino terminus, allowing selective deprotection under mild acidic conditions, while the ester functionalities safeguard the side chain and C-terminus, facilitating precise stepwise assembly of complex peptide chains. It is widely used in solid-phase peptide synthesis and the development of enzyme inhibitors or receptor ligands.

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