(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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿8,400.00
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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