Bromoacetamido-PEG4-C2-Boc

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Reagent Code: #121112
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CAS Number 1807521-00-1

science Other reagents with same CAS 1807521-00-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 442.34 g/mol
Formula C₁₇H₃₂BrNO₇
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in bioconjugation and peptide synthesis. It serves as a protective group for amines during the synthesis of complex molecules, ensuring selective reactions at specific sites. The PEG4 spacer enhances solubility and flexibility, making it suitable for modifying biomolecules like proteins and peptides. Additionally, it is employed in the development of drug delivery systems, where it helps in creating stable and targeted conjugates. Its Boc group can be easily removed under mild acidic conditions, allowing for further functionalization in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿23,040.00
inventory 5mg
10-20 days ฿66,240.00

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Bromoacetamido-PEG4-C2-Boc
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This chemical is primarily used in bioconjugation and peptide synthesis. It serves as a protective group for amines during the synthesis of complex molecules, ensuring selective reactions at specific sites. The PEG4 spacer enhances solubility and flexibility, making it suitable for modifying biomolecules like proteins and peptides. Additionally, it is employed in the development of drug delivery systems, where it helps in creating stable and targeted conjugates. Its Boc group can be easily removed under

This chemical is primarily used in bioconjugation and peptide synthesis. It serves as a protective group for amines during the synthesis of complex molecules, ensuring selective reactions at specific sites. The PEG4 spacer enhances solubility and flexibility, making it suitable for modifying biomolecules like proteins and peptides. Additionally, it is employed in the development of drug delivery systems, where it helps in creating stable and targeted conjugates. Its Boc group can be easily removed under mild acidic conditions, allowing for further functionalization in multi-step synthetic processes.

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