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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque Genkwanin - ≥97% , CAS No.437-64-9
Disponível para encomenda
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 Sinónimos
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%
Especificações e pureza
≥97%
Mecanismos bioquímicos e fisiológicos
Genkwanin is a non-glycosylated flavonoid found in many herbs. It is an antitumor constituent and has anti-inflammatory activities.
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Pubchem Sid 528775124 Sorrisos canónicos 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 SMILES isoméricas COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O Peso molecular 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 Descrição 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.
Estrutura 3D Alvos associados (humanos) Alvos associados (não humanos) Mecanismos de ação Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e físicas Solubilidade Acetone (Very Slightly, Sonicated), DMSO (Slightly), Methanol (Slightly, Heated) Sensibilidade Hygroscopic.light sensitive Ponto de fusão (°C) 286.0-292.0°C Peso molecular 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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