2,3,4,5,6-pentafluorophenyl 1-[(4-formylphenyl)formamido]-3,6,9,12-tetraoxapentadecan-15-oate

98%

Reagent Code: #223202
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CAS Number 1324007-10-4

science Other reagents with same CAS 1324007-10-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 563.47 g/mol
Formula C₂₅H₂₆F₅NO₈
badge Registry Numbers
MDL Number MFCD22201546
thermostat Physical Properties
Boiling Point 658.6±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.346±0.06 g/cm3(Predicted)
Storage -20°C

description Product Description

Used in advanced organic synthesis, particularly as a highly specialized linker in solid-phase peptide synthesis and bioconjugation. Its pentafluorophenyl ester group enables efficient and selective coupling with primary amines under mild conditions, making it valuable for constructing peptide arrays and functionalizing biomolecules. The aldehyde functionality allows for further modification via reductive amination or oxime ligation, enabling modular assembly of complex molecular architectures. The tetraethylene glycol spacer provides hydrophilicity and flexibility, reducing aggregation and improving solubility in aqueous and organic media—ideal for creating bioactive conjugates, sensors, and functionalized surfaces in diagnostic and pharmaceutical research.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿39,980.00

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2,3,4,5,6-pentafluorophenyl 1-[(4-formylphenyl)formamido]-3,6,9,12-tetraoxapentadecan-15-oate
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Used in advanced organic synthesis, particularly as a highly specialized linker in solid-phase peptide synthesis and bioconjugation. Its pentafluorophenyl ester group enables efficient and selective coupling with primary amines under mild conditions, making it valuable for constructing peptide arrays and functionalizing biomolecules. The aldehyde functionality allows for further modification via reductive amination or oxime ligation, enabling modular assembly of complex molecular architectures. The tetra

Used in advanced organic synthesis, particularly as a highly specialized linker in solid-phase peptide synthesis and bioconjugation. Its pentafluorophenyl ester group enables efficient and selective coupling with primary amines under mild conditions, making it valuable for constructing peptide arrays and functionalizing biomolecules. The aldehyde functionality allows for further modification via reductive amination or oxime ligation, enabling modular assembly of complex molecular architectures. The tetraethylene glycol spacer provides hydrophilicity and flexibility, reducing aggregation and improving solubility in aqueous and organic media—ideal for creating bioactive conjugates, sensors, and functionalized surfaces in diagnostic and pharmaceutical research.

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