2, 5-Dioxopyrrolidin-1-yl 4-(1, 2, 2-triphenylvinyl)benzoate

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Reagent Code: #177938
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CAS Number 2001537-57-9

science Other reagents with same CAS 2001537-57-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 473.52 g/mol
Formula C₃₁H₂₃NO₄
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

Used as a fluorescent labeling reagent in bioconjugation and bioimaging applications. Its aggregation-induced emission (AIE) properties make it highly effective for tracking biomolecules in aqueous environments, where traditional fluorophores often quench. The active ester group readily reacts with primary amines on proteins, peptides, or amine-modified nucleic acids, forming stable amide bonds. This allows for efficient and specific labeling of biomolecules without the need for catalysts. Due to the triphenylvinyl group, it exhibits strong fluorescence upon binding to macromolecules or in hydrophobic environments, enabling sensitive detection in cellular imaging and diagnostic assays. Also employed in the development of AIE-based sensors and probes for monitoring biological processes in real time.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,400.00
inventory 250mg
10-20 days ฿3,840.00
inventory 1g
10-20 days ฿9,530.00

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2, 5-Dioxopyrrolidin-1-yl 4-(1, 2, 2-triphenylvinyl)benzoate
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Used as a fluorescent labeling reagent in bioconjugation and bioimaging applications. Its aggregation-induced emission (AIE) properties make it highly effective for tracking biomolecules in aqueous environments, where traditional fluorophores often quench. The active ester group readily reacts with primary amines on proteins, peptides, or amine-modified nucleic acids, forming stable amide bonds. This allows for efficient and specific labeling of biomolecules without the need for catalysts. Due to the tri

Used as a fluorescent labeling reagent in bioconjugation and bioimaging applications. Its aggregation-induced emission (AIE) properties make it highly effective for tracking biomolecules in aqueous environments, where traditional fluorophores often quench. The active ester group readily reacts with primary amines on proteins, peptides, or amine-modified nucleic acids, forming stable amide bonds. This allows for efficient and specific labeling of biomolecules without the need for catalysts. Due to the triphenylvinyl group, it exhibits strong fluorescence upon binding to macromolecules or in hydrophobic environments, enabling sensitive detection in cellular imaging and diagnostic assays. Also employed in the development of AIE-based sensors and probes for monitoring biological processes in real time.

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