(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-vinylphenyl)propanoic acid

95%

Reagent Code: #236638
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CAS Number 1270295-57-2

science Other reagents with same CAS 1270295-57-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 413.47 g/mol
Formula C₂₆H₂₃NO₄
badge Registry Numbers
MDL Number MFCD09951904
inventory_2 Storage & Handling
Storage Room temperature, sealed, light-proof

description Product Description

Used in peptide synthesis as a chiral building block for introducing phenylalanine derivatives with a vinyl-functionalized side chain. The vinyl group allows for post-synthetic modifications via cross-coupling reactions or polymerization, making it valuable in the development of functionalized biomaterials, bioconjugates, or stimuli-responsive peptides. The Fmoc protection enables compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly of custom sequences under mild basic conditions. Its stereochemistry ensures enantioselective incorporation, which is critical for maintaining biological activity in synthetic peptides.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,400.00
inventory 250mg
10-20 days ฿33,580.00
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-vinylphenyl)propanoic acid
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Used in peptide synthesis as a chiral building block for introducing phenylalanine derivatives with a vinyl-functionalized side chain. The vinyl group allows for post-synthetic modifications via cross-coupling reactions or polymerization, making it valuable in the development of functionalized biomaterials, bioconjugates, or stimuli-responsive peptides. The Fmoc protection enables compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly of custom sequences under mild b

Used in peptide synthesis as a chiral building block for introducing phenylalanine derivatives with a vinyl-functionalized side chain. The vinyl group allows for post-synthetic modifications via cross-coupling reactions or polymerization, making it valuable in the development of functionalized biomaterials, bioconjugates, or stimuli-responsive peptides. The Fmoc protection enables compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly of custom sequences under mild basic conditions. Its stereochemistry ensures enantioselective incorporation, which is critical for maintaining biological activity in synthetic peptides.

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