2,3,4,5,6-pentafluorophenyl 4-methyl-4-(pyridin-2-yldisulfanyl)pentanoate

98%

Reagent Code: #223190
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CAS Number 2101206-44-2

science Other reagents with same CAS 2101206-44-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 423.42 g/mol
Formula C₁₇H₁₄F₅NO₂S₂
badge Registry Numbers
MDL Number MFCD28556932
thermostat Physical Properties
Boiling Point 460.5±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.43±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in advanced organic synthesis as a highly specialized activating agent for carboxylic acids, particularly in peptide coupling and polymer chemistry. Its unique pentafluorophenyl ester group enhances reactivity due to strong electron-withdrawing effects, enabling efficient acylation under mild conditions. The disulfide-pyridine moiety allows for reversible conjugation and potential redox-responsive behavior, making it valuable in designing stimuli-responsive biomaterials and drug delivery systems. Frequently employed in surface functionalization and bioconjugation where controlled reactivity and stability are required.

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inventory 100mg
10-20 days ฿37,950.00

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2,3,4,5,6-pentafluorophenyl 4-methyl-4-(pyridin-2-yldisulfanyl)pentanoate
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Used in advanced organic synthesis as a highly specialized activating agent for carboxylic acids, particularly in peptide coupling and polymer chemistry. Its unique pentafluorophenyl ester group enhances reactivity due to strong electron-withdrawing effects, enabling efficient acylation under mild conditions. The disulfide-pyridine moiety allows for reversible conjugation and potential redox-responsive behavior, making it valuable in designing stimuli-responsive biomaterials and drug delivery systems. Fr

Used in advanced organic synthesis as a highly specialized activating agent for carboxylic acids, particularly in peptide coupling and polymer chemistry. Its unique pentafluorophenyl ester group enhances reactivity due to strong electron-withdrawing effects, enabling efficient acylation under mild conditions. The disulfide-pyridine moiety allows for reversible conjugation and potential redox-responsive behavior, making it valuable in designing stimuli-responsive biomaterials and drug delivery systems. Frequently employed in surface functionalization and bioconjugation where controlled reactivity and stability are required.

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