CAS 305-01-1
:Esculetin
- (2-Chlorophenyl)(Phenyl)Methanone
- 2H-1-Benzopyran-2-one, 6,7-dihydroxy-
- 6,7-Dihidroxi-2-Benzopirona
- 6,7-Dihydroxy-2-Benzopyrone
- 6,7-Dihydroxy-2-benzopyron
- 6,7-Dihydroxy-2H-1-benzopyran-2-one
- 6,7-Dihydroxycoumarin
- Aesculetin
- Asculetine
- Cichorigenin
- Cichoriin aglycon
- Coumarin, 6,7-dihydroxy-
- Esculetin
- Esculetol
- Esculin aglycon
- See more synonyms
Esculetin
CAS:Formula:C9H6O4Purity:>98.0%(T)(HPLC)Color and Shape:Light yellow to Brown to Dark green powder to crystalMolecular weight:178.14Esculetin
CAS:Esculetin analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C9H6O4Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:178.15ESCULETIN CRS
CAS:ESCULETIN CRSFormula:C13H9ClOColor and Shape:Yellow. Powder.Molecular weight:216.6632H-1-Benzopyran-2-one, 6,7-dihydroxy-
CAS:Formula:C9H6O4Purity:95%Color and Shape:SolidMolecular weight:178.1415Esculetin
CAS:EsculetinFormula:C9H6O4Purity:> 95 % nmr (Typical Value in Batch COA)Color and Shape: faint yellow powderMolecular weight:178.14g/molEsculetin [Matrix for MALDI-TOF/MS]
CAS:Formula:C9H6O4Purity:>99.0%(T)(HPLC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:178.14Esculetin
CAS:Esculetin: a coumarin from plants with anti-edema, anti-inflammatory, anti-tumor properties; inhibits LOs.Formula:C9H6O4Purity:98.03% - 99.76%Color and Shape:Yellow Crystalline PowderMolecular weight:178.14Esculetin
CAS:LactoneFormula:C9H6O4Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:178.146,7-Dihydroxycoumarin (Esculetin)
CAS:Formula:C9H6O4Color and Shape:Light YellowMolecular weight:178.14Esculetin
CAS:Esculetin is a naturally occurring coumarin compound, which is predominantly derived from various plant sources, such as the bark and leaves of certain trees and shrubs. As a member of the coumarin family, it is characterized by its benzopyrone structure and is often isolated from botanicals through organic solvent extraction methods.
Its mode of action primarily involves its ability to scavenge free radicals and chelate metal ions, contributing to its notable antioxidant capacity. Furthermore, Esculetin exerts anti-inflammatory effects by inhibiting the activity of enzymes such as cyclooxygenase and lipoxygenase, which are integral to the inflammatory pathway.
Common applications of Esculetin are found in scientific research where it is utilized for its potential therapeutic properties. Studies have investigated its role in modulating oxidative stress, its protective effects in neurodegenerative disorders, and its capability to inhibit the proliferation of certain cancer cell lines. Additionally, it serves as a useful biochemical tool in elucidating the pathways of inflammation and oxidative stress within cellular models. Scientists continue to explore its potential as a lead compound in drug discovery and development.Formula:C9H6O4Purity:Min. 98.0 Area-%Molecular weight:178.15 g/mol6,7-Dihydroxy-2H-chromen-2-one
CAS:Formula:C9H6O4Purity:95%Color and Shape:SolidMolecular weight:178.143











