
CAS 5054-59-1
:2-(2,6-dioxopiperidin-3-yl)-4-hydroxyisoindoline-1,3-dione
Description:
2-(2,6-Dioxopiperidin-3-yl)-4-hydroxyisoindoline-1,3-dione, with the CAS number 5054-59-1, is a chemical compound that features a complex structure characterized by a piperidine ring and an isoindoline moiety. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar organic solvents. The presence of multiple functional groups, including carbonyl and hydroxyl groups, suggests that it may engage in hydrogen bonding, influencing its reactivity and interactions with other molecules. Its dioxopiperidine structure may contribute to its biological activity, potentially making it of interest in medicinal chemistry. The compound's unique arrangement of atoms and functional groups can lead to specific chemical behaviors, such as reactivity in condensation reactions or as a potential ligand in coordination chemistry. Overall, 2-(2,6-dioxopiperidin-3-yl)-4-hydroxyisoindoline-1,3-dione represents a fascinating subject for further research in both synthetic and applied chemistry contexts.
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Found 8 products.
2-(2,6-Dioxopiperidin-3-yl)-4-hydroxyisoindoline-1,3-dione
CAS:Formula:C13H10N2O5Purity:>98.0%(T)(HPLC)Color and Shape:White to Yellow powder to crystalMolecular weight:274.23Thalidomide-4-OH
CAS:<p>Thalidomide-4-OH, a Thalidomide-derived Cereblon binder, recruits CRBN and serves as a PROTAC linker.</p>Formula:C13H10N2O5Purity:99.59%Color and Shape:SolidMolecular weight:274.233-Hydroxy thalidomide
CAS:<p>3-Hydroxy thalidomide is a drug that is used to treat cancer. It is an inhibitor of the ubiquitin-proteasome system and inhibits the growth of cancer cells. It has been shown to inhibit the proliferation of prostate cancer cells in culture, as well as inhibiting the growth of rat liver microsomes. 3-Hydroxy thalidomide has been shown to be suitable for oral administration and it has a long half-life, making it suitable for treatment in patients who cannot tolerate other drugs. 3-Hydroxy thalidomide also inhibits the growth factor basic fibroblast growth factor (bFGF), which may contribute to its anti-cancer effects.</p>Formula:C13H10N2O5Purity:Min. 98 Area-%Color and Shape:Yellow PowderMolecular weight:274.23 g/mol2-(2,6-Dioxopiperidin-3-yl)-4-hydroxyisoindoline-1,3-dione
CAS:Formula:C13H10N2O5Purity:95%Color and Shape:Solid, No data available.Molecular weight:274.232






