Boc-Pro-Phe-OH

≥95%

Reagent Code: #38070
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CAS Number 52071-65-5

science Other reagents with same CAS 52071-65-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.42 g/mol
Formula C₁₉H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD00237581
thermostat Physical Properties
Boiling Point 578.5±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily used in peptide synthesis as a protected dipeptide. It serves as a building block in the creation of more complex peptide chains, where the Boc (tert-butyloxycarbonyl) group protects the amino group during the synthesis process. This protection prevents unwanted side reactions, ensuring the correct sequence of amino acids in the final peptide product. It is particularly useful in solid-phase peptide synthesis (SPPS), a common method for producing peptides in research and pharmaceutical applications. After the peptide chain is assembled, the Boc group can be removed under acidic conditions, allowing further modifications or the completion of the peptide structure. Its application is crucial in developing therapeutic peptides, studying protein functions, and designing bioactive molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,852.00
inventory 250mg
10-20 days ฿1,926.00

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Boc-Pro-Phe-OH
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This compound is primarily used in peptide synthesis as a protected dipeptide. It serves as a building block in the creation of more complex peptide chains, where the Boc (tert-butyloxycarbonyl) group protects the amino group during the synthesis process. This protection prevents unwanted side reactions, ensuring the correct sequence of amino acids in the final peptide product. It is particularly useful in solid-phase peptide synthesis (SPPS), a common method for producing peptides in research and pharma

This compound is primarily used in peptide synthesis as a protected dipeptide. It serves as a building block in the creation of more complex peptide chains, where the Boc (tert-butyloxycarbonyl) group protects the amino group during the synthesis process. This protection prevents unwanted side reactions, ensuring the correct sequence of amino acids in the final peptide product. It is particularly useful in solid-phase peptide synthesis (SPPS), a common method for producing peptides in research and pharmaceutical applications. After the peptide chain is assembled, the Boc group can be removed under acidic conditions, allowing further modifications or the completion of the peptide structure. Its application is crucial in developing therapeutic peptides, studying protein functions, and designing bioactive molecules.

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