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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag auf Lager eupatorin-5-methyl ether - Reagent grade , CAS No.21764-09-0
GRADE & PURITY Reagent Grade ? General reagent-grade purity suitable for most laboratory work. Use as a dependable default when no specific higher grade is required. Synonyms
3'-Hydroxy-5,6,7,4'-tetramethoxyflavone | MFCD00016928 | SCHEMBL1764630 | 6-Hydroxyluteolin 5,6,7,4'-tetramethyl ether | 2-(3-hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one | AKOS024286205 | 2-(3-Hydroxy-4-methoxy-phenyl)-5,6,7-trimethoxy-chro
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Why this grade Reagent grade Reagent Grade for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature Ships Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyme
3'-Hydroxy-5,6,7,4'-tetramethoxyflavone | MFCD00016928 | SCHEMBL1764630 | 6-Hydroxyluteolin 5,6,7,4'-tetramethyl ether | 2-(3-hydroxy-4-methoxyphenyl)-5,6,7-trimethoxy-4H-chromen-4-one | AKOS024286205 | 2-(3-Hydroxy-4-methoxy-phenyl)-5,6,7-trimethoxy-chro
Spezifikationen & Reinheit
Reagent grade
Namen und Kennungen Kanonisches Lächeln COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)O IUPAC Name 2-(3-hydroxy-4-methoxyphenyl)-5,6,7-trimethoxychromen-4-one InChIKey LYLDPYNWDVVPIQ-UHFFFAOYSA-N INCHI 1S/C19H18O7/c1-22-13-6-5-10(7-11(13)20)14-8-12(21)17-15(26-14)9-16(23-2)18(24-3)19(17)25-4/h5-9,20H,1-4H3 Isomere SMILES COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)O UN-Nummer 2811 Molekulargewicht 358.34 Reaxy-Rn 5626139 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=5626139&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Phenylpropanoids and polyketides Klasse Flavonoids Subclass O-methylated flavonoids Intermediate Tree Nodes Not available Direct Parent 7-O-methylated flavonoids Alternative Parents 4'-O-methylated flavonoids 5-O-methylated flavonoids 6-O-methylated flavonoids 3'-hydroxyflavonoids Monohydroxyflavonoids Flavones Chromones Methoxyphenols Phenoxy compounds Methoxybenzenes Anisoles 1-hydroxy-2-unsubstituted benzenoids Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Vinylogous esters Heteroaromatic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 4p-methoxyflavonoid-skeleton - 5-methoxyflavonoid-skeleton - 6-methoxyflavonoid-skeleton - 7-methoxyflavonoid-skeleton - 3'-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Monohydroxyflavonoid - Chromone - Benzopyran - Methoxyphenol - 1-benzopyran - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - 1-hydroxy-2-unsubstituted benzenoid - Pyranone - Phenol - 1-hydroxy-4-unsubstituted benzenoid - Alkyl aryl ether - Benzenoid - Pyran - Monocyclic benzene moiety - Vinylogous ester - Heteroaromatic compound - Organoheterocyclic compound - Oxacycle - Ether - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound Beschreibung This compound belongs to the class of organic compounds known as 7-o-methylated flavonoids. These are flavonoids with methoxy groups attached to the C7 atom of the flavonoid backbone. External Descriptors Flavones and Flavonols Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Flammpunkt (°F) Not applicable Flammpunkt (°C) Not applicable Molekulargewicht 358.300 g/mol XLogP3 2.700 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 5 Exact Mass 358.105 Da Monoisotopic Mass 358.105 Da Topological Polar Surface Area 83.500 Ų Heavy Atom Count 26 Formal Charge 0 Complexity 534.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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