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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Genkwanin - ≥97% , CAS No.437-64-9
Synonyms
NCGC00178332-02 | Spectrum5_000573 | Flavone, 4',5-dihydroxy-7-methoxy- | CHEBI:75718 | KBioSS_000810 | n-2,4-dimethylphenyl-n-methylformamidine | s9287 | 5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one | AKOS015896775 | C10046 | Genkwanin, >=98%
Shipped In
Ice chest + Ice pads
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Why this grade ≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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 Synonymes
NCGC00178332-02 | Spectrum5_000573 | Flavone, 4',5-dihydroxy-7-methoxy- | CHEBI:75718 | KBioSS_000810 | n-2,4-dimethylphenyl-n-methylformamidine | s9287 | 5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4H-chromen-4-one | AKOS015896775 | C10046 | Genkwanin, >=98%
Spécifications et pureté
≥97%
Mécanismes biochimiques et physiologiques
Genkwanin is a non-glycosylated flavonoid found in many herbs. It is an antitumor constituent and has anti-inflammatory activities.
Conditions de stockage de stockage
Store at -20°C
Expédié en
Ice chest + Ice pads
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Noms et identifiants Pubchem Sid 528775124 Sourires canoniques COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O IUPAC Name 5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one InChIKey JPMYFOBNRRGFNO-UHFFFAOYSA-N INCHI 1S/C16H12O5/c1-20-11-6-12(18)16-13(19)8-14(21-15(16)7-11)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3 Isomères SMILES COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O Poids moléculaire 284.26 Reaxy-Rn 292549 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=292549&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 Classe Flavonoids Subclass O-methylated flavonoids Intermediate Tree Nodes Not available Direct Parent 7-O-methylated flavonoids Alternative Parents Flavones 5-hydroxyflavonoids 4'-hydroxyflavonoids Chromones Anisoles Pyranones and derivatives Alkyl aryl ethers 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Vinylogous acids Heteroaromatic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteropolycyclic compounds Substituents 7-methoxyflavonoid-skeleton - 4'-hydroxyflavonoid - 5-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Chromone - Benzopyran - 1-benzopyran - Anisole - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Pyranone - Phenol - Monocyclic benzene moiety - Benzenoid - Pyran - Vinylogous acid - Heteroaromatic compound - Ether - Organoheterocyclic compound - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic heteropolycyclic compound Description 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.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité Acetone (Very Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly, Heated) Sensibilité Hygroscopic.light sensitive Point de fusion (°C) 286.0-292.0°C Poids moléculaire 284.260 g/mol XLogP3 2.100 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 5 Rotatable Bond Count 2 Exact Mass 284.068 Da Monoisotopic Mass 284.068 Da Topological Polar Surface Area 76.000 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 424.000 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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