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Usage

Uses

Used in Organic Synthesis:
2,5-Pyrrolidinedione, 1-[(1-pyrenylacetyl)oxy]is used as a starting material in organic synthesis for the preparation of other compounds. Its complex structure allows for the creation of a variety of chemical entities, making it a valuable component in the synthesis process.
Used in Dye Development:
2,5-Pyrrolidinedione, 1-[(1-pyrenylacetyl)oxy]is used as a precursor in the development of dyes due to the fluorescence properties of the pyrene group. This characteristic makes it suitable for creating dyes with specific optical properties, which can be tailored for various applications.
Used in Fluorescent Labeling:
2,5-Pyrrolidinedione, 1-[(1-pyrenylacetyl)oxy]is used as a component in fluorescent labels for its ability to emit light. This feature is particularly useful in biological and chemical research, where fluorescent labels can help in tracking and visualizing specific molecules or processes.
Used in Medicinal Chemistry:
Although further research is needed, the compound may have potential applications in medicinal chemistry. Its unique structure and properties could be harnessed to develop new pharmaceutical agents or improve existing ones.
Used in Material Science:
2,5-Pyrrolidinedione, 1-[(1-pyrenylacetyl)oxy]-'s potential uses in material science are still being explored. Its structural and fluorescent characteristics could contribute to the development of new materials with specialized properties for various applications.

Upstream product

• 6066-82-6 1-hydroxy-pyrrolidine-2,5-dione 
• 64709-55-3 1-pyreneacetic acid 
• 72425-17-3 1-pyreneacetyl chloride 

Relevant academic research and scientific papers

Sensitized luminescence emission of the europium(III) ion bound to a pyrene-containing triacid ligand

A pyrene-tethered triacid receptor and its chelates with two lanthanide(III) metal cations have been synthesized. The first example of energy transfer taking place from the excited pyrene chromophore to the europium(III) metal is reported therein.

Synthesis, antimicrobial activity, attenuation of aminoglycoside resistance in MRSA, and ribosomal A-site binding of pyrene-neomycin conjugates

The development of new ligands that have comparable or enhanced therapeutic efficacy relative to current drugs is vital to the health of the global community in the short and long term. One strategy to accomplish this goal is to functionalize sites on cur

Cu2+-selective turn-on fluorescence signaling based on metal-induced hydrolysis of pyrenecarbohydrazide

We developed a simple Cu2+-selective turn-on fluorescence signaling probe based on the hydrolysis of 1-pyrenecarbohydrazide (1) to 1-pyrenecarboxylic acid. Probe 1 exhibited prominent fluorescence signaling of Cu2+ ions in a 10% aqueous Tris-buffered (pH 7.0) DMSO solution with a detection limit of 5.93?×?10?8?M. Signaling with control compounds derived from pyreneacetic acid and pyrenebutyric acid showed that the fluorescence signal became less pronounced as the distance between the hydrazide functionality and the pyrene fluorophore increased. As a practical application, this probe was employed for the determination of Cu2+ in a simulated semiconductor wastewater.

Molecularly imprinted polymers as antibody mimics in automated on-line fluorescent competitive assays

An automated molecularly imprinted sorbent based assay (MIA) for the rapid and sensitive analysis of penicillin-type β-lactam antibiotics (BLAs) has been developed and optimized. The polymers were prepared using penicillin G procaine salt as template (PEN

Molecular engineering of fluorescent penicillins for molecularly imprinted polymer assays

The interaction of seven novel fluorescent labeled β-lactams with a library of six polymer materials molecularly imprinted (MI) with penicillin G (PenG) has been evaluated using both radioactive and fluorescence competitive assays. The highly fluorescent