2,5-dioxopyrrolidin-1-yl 4-formylbenzoate - CAS 60444-78-2

2,5-dioxopyrrolidin-1-yl 4-formylbenzoate - CAS 60444-78-2 Catalog number: BADC-00365

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2,5-dioxopyrrolidin-1-yl 4-formylbenzoate is a vital compound used in the biomedical industry. It exhibits remarkable potential for the treatment of various diseases, particularly inflammatory disorders. Its unique chemical structure makes it a promising candidate for developing drugs that target specific molecular pathways involved in inflammation.

Category
ADCs Linker
Product Name
2,5-dioxopyrrolidin-1-yl 4-formylbenzoate
CAS
60444-78-2
Catalog Number
BADC-00365
Molecular Formula
C12H9NO5
Molecular Weight
247.20
2,5-dioxopyrrolidin-1-yl 4-formylbenzoate

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Description
2,5-dioxopyrrolidin-1-yl 4-formylbenzoate is a vital compound used in the biomedical industry. It exhibits remarkable potential for the treatment of various diseases, particularly inflammatory disorders. Its unique chemical structure makes it a promising candidate for developing drugs that target specific molecular pathways involved in inflammation.
Synonyms
(2,5-dioxopyrrolidin-1-yl) 4-formylbenzoate;
IUPAC Name
(2,5-dioxopyrrolidin-1-yl) 4-formylbenzoate
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)C2=CC=C(C=C2)C=O
InChI
InChI=1S/C12H9NO5/c14-7-8-1-3-9(4-2-8)12(17)18-13-10(15)5-6-11(13)16/h1-4,7H,5-6H2
InChIKey
VHYRHFNOWKMCHQ-UHFFFAOYSA-N
Density
1.44 g/cm3
LogP
0.65780
Appearance
Soild powder
Purity
≥ 98 %
Shipping
Room temperature, or blue ice upon request.
Boiling Point
425.4 °C at 760 mmHg

2.5-Dioxopyrrolidin-1-yl 4-formylbenzoate, a highly versatile chemical compound extensively employed in biochemical research and applications, showcases a myriad of key applications, presented with a high degree of perplexity and burstiness:

Bioconjugation: Serving as the linchpin in chemical bioconjugation methods, this compound acts as the adhesive, binding biomolecules like proteins, peptides, and nucleic acids with diverse tags or labels. The strategic presence of the formyl group enables seamless conjugation with amine-containing molecules through Schiff base formation, playing a crucial role in crafting biomolecule conjugates essential for diagnostic, therapeutic, and research endeavors.

Surface Functionalization: Delving into the realm of surface functionalization, 2.5-Dioxopyrrolidin-1-yl 4-formylbenzoate emerges as a key architect in shaping surfaces of nanoparticles, microarrays, or biosensors. By anchoring this compound onto surfaces, researchers introduce reactive aldehyde groups capable of binding to specific biomolecules, thus enhancing the detection sensitivity and specificity of biosensing platforms with finesse.

Chemical Synthesis: Within the intricate world of synthetic chemistry, this compound takes the spotlight as a potent intermediate or reagent utilized in creating a diverse array of chemical entities. Its reactive formyl group engages in numerous chemical reactions, such as condensation, cyclization, and reduction, facilitating the synthesis of complex organic molecules essential for advancements in drug discovery and material science.

Drug Delivery Systems: Positioned at the forefront of cutting-edge drug delivery system design, the utilization of this compound demonstrates its efficacy in forming stable conjugates with therapeutic agents. Binding drugs to 2,5-dioxopyrrolidin-1-yl 4-formylbenzoate empowers scientists to develop prodrugs or drug carriers that enhance drug solubility, stability, and targeted delivery, thereby enhancing the therapeutic efficacy and safety profile of pharmaceuticals to unprecedented levels.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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