5-Hydroxyflavone - ≥98%(HPLC) , CAS No.491-78-1

Name: 5-Hydroxyflavone - ≥98%(HPLC) , CAS No.491-78-1
Brand: Aladdin Scientific
SKU: H157353
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CAS: 491-78-1 Cat. No.: H157353 Summenformel: C₁₅H₁₀O₃ Molekulargewicht: 238.24 Beilstein Registry Number: 18(5)2,254 EG-Nummer: 207-743-1

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QUALITÄT & REINHEIT ≥98%(HPLC)

Synonyms

Storage

Room temperature,Argon charged

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Spezifikationen Namen und Kennungen Dokumentation Erweiterte Daten Taxonomic Classification 3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften FAQs und Artikel Citations of This Product Lösungsrechner Bewertungen

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Warum diese Qualität

≥98%(HPLC) für empfindliche chromatographische und analytische Workflows, die minimale Basislinieninterferenzen erfordern.

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Room temperature,Argon charged Versand Normal. Genaue Spezifikationen finden Sie im chargenspezifischen COA.

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SDS, COA, Datenblatt und Spezifikationsblatt stehen zum Download bereit. Chargenspezifische COA über Chargennummernsuche abrufbar.

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Literaturbeleg

In 3 peer-reviewten Publikationen zu Chromatographie, organischer Synthese und Kreuzkupplungsreaktionen zitiert.

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Synonyme

Spezifikationen & Reinheit

≥98%(HPLC)

Storage

Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥98%(HPLC)

Namen und Kennungen

Pubchem Sid

488184085

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488184085

Kanonisches Lächeln

C1=CC=C(C=C1)C2=CC(=O)C3=C(C=CC=C3O2)O

IUPAC Name

5-hydroxy-2-phenylchromen-4-one

InChIKey

IYBLVRRCNVHZQJ-UHFFFAOYSA-N

INCHI

1S/C15H10O3/c16-11-7-4-8-13-15(11)12(17)9-14(18-13)10-5-2-1-3-6-10/h1-9,16H

Isomere SMILES

C1=CC=C(C=C1)C2=CC(=O)C3=C(C=CC=C3O2)O

WGK Deutschland

Molekulargewicht

238.24

Beilstein

18(5)2,254

Reaxy-Rn

194429

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=194429&ln=

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Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Phenylpropanoids and polyketides
  - Klasse Flavonoids
    - Subclass Flavones

Kingdom	Organic compounds
Superclass	Phenylpropanoids and polyketides
Klasse	Flavonoids
Subclass	Flavones
Intermediate Tree Nodes	Not available
Direct Parent	Flavones
Alternative Parents	5-hydroxyflavonoids Chromones Pyranones and derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Benzene and substituted derivatives Vinylogous acids Heteroaromatic compounds Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	5-hydroxyflavonoid - Flavone - Hydroxyflavonoid - Chromone - Benzopyran - 1-benzopyran - Pyranone - 1-hydroxy-2-unsubstituted benzenoid - 1-hydroxy-4-unsubstituted benzenoid - Benzenoid - Pyran - Monocyclic benzene moiety - Vinylogous acid - Heteroaromatic compound - Oxacycle - Organoheterocyclic compound - Organooxygen compound - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Aromatic heteropolycyclic compound
Beschreibung	This compound belongs to the class of organic compounds known as flavones. These are flavonoids with a structure based on the backbone of 2-phenylchromen-4-one (2-phenyl-1-benzopyran-4-one).
External Descriptors	Flavones and Flavonols
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. DOI: 10.1186/s13321-016-0174-y

3D-Struktur

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CYP1A2 Tchem Cytochrome P450 1A2 (1 Activities)

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CYP1B1 Tchem Cytochrome P450 1B1 (1 Activities)

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NR3C1 Tclin Glucocorticoid receptor (14987 Activities)

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ALOX5 Tclin Arachidonate 5-lipoxygenase (6568 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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TOP2A Tclin DNA topoisomerase II alpha (6317 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)

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AKR1B1 Tclin Aldose reductase (1404 Activities)

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ADORA2A Tclin Adenosine A2a receptor (16305 Activities)

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ADORA3 Tchem Adenosine A3 receptor (15931 Activities)

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CYP1B1 Tchem Cytochrome P450 1B1 (1148 Activities)

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NEU2 Tbio Sialidase 2 (382 Activities)

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GBA1 Tclin Beta-glucocerebrosidase (14647 Activities)

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CYP1A1 Tchem Cytochrome P450 1A1 (1169 Activities)

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ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

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FBP1 Tchem Fructose-1,6-bisphosphatase (1199 Activities)

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FASN Tchem Fatty acid synthase (3390 Activities)

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ALOX15 Tchem Arachidonate 15-lipoxygenase (7108 Activities)

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CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)

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CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)

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K562 (73714 Activities)

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MCF7 (126967 Activities)

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HepG2 (196354 Activities)

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KB (17409 Activities)

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GNAS Tbio Guanine nucleotide-binding protein G(s), subunit alpha (103405 Activities)

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POLI Tchem DNA polymerase iota (116820 Activities)

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AKR1B10 Tchem Aldo-keto reductase family 1 member B10 (300 Activities)

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SMN1 Tchem Survival motor neuron protein (34246 Activities)

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GMNN Tbio Geminin (128009 Activities)

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RGS4 Tchem Regulator of G-protein signaling 4 (13867 Activities)

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MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)

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TARDBP Tchem TAR DNA-binding protein 43 (40113 Activities)

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Pkm Pyruvate kinase isozymes M1/M2 (66 Activities)

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Salmonella typhimurium (15756 Activities)

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Trypanosoma brucei brucei (13300 Activities)

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Plasmodium falciparum (966862 Activities)

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Rattus norvegicus (775804 Activities)

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CCRF S-180 (1031 Activities)

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Lewis lung carcinoma cell line (1243 Activities)

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fabG 3-oxoacyl-acyl-carrier protein reductase (70 Activities)

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fabI Enoyl-acyl-carrier protein reductase (415 Activities)

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Mapt Microtubule-associated protein tau (6 Activities)

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Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

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Ntrk2 BDNF/NT-3 growth factors receptor (124 Activities)

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Gabrp GABA-A receptor; anion channel (5731 Activities)

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SARS-CoV-2 (38078 Activities)

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Wirkungsmechanismen

Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)

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9 results found

Lot Number	Certificate Type	Datum	Artikel
I2608139	Certificate of Analysis	Sep 12, 2026	H157353
B2209255	Certificate of Analysis	Oct 30, 2025	H157353
B2209257	Certificate of Analysis	Oct 30, 2025	H157353
B2209258	Certificate of Analysis	Oct 30, 2025	H157353
B2209259	Certificate of Analysis	Oct 30, 2025	H157353
B2209261	Certificate of Analysis	Oct 30, 2025	H157353
B2209264	Certificate of Analysis	Oct 30, 2025	H157353
K2110738	Certificate of Analysis	Aug 12, 2025	H157353
F2129280	Certificate of Analysis	Apr 08, 2025	H157353

Chemische und physikalische Eigenschaften

Empfindlichkeit	Air sensitive
Schmelzpunkt (°C)	157-161℃
Molekulargewicht	238.240 g/mol
XLogP3	2.500
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	1
Exact Mass	238.063 Da
Monoisotopic Mass	238.063 Da
Topological Polar Surface Area	46.500 Å²
Heavy Atom Count	18
Formal Charge	0
Complexity	355.000
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

FAQs und Artikel

Flavones: Structural Features, Physicochemical Properties, and Key Points for Research and Applications

Categories: Technical Articles: Reagent Chemistry, Synthesis & Bioscience Guides

Tags:

HPLC Antioxidation flavone C6–C3–C6 flavone glycosides O-glycosides C-glycosides C5-hydroxylation 5-deoxy flavones TLR/NF-κB heterologous biosynthesis

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Organic synthesis — reaction medium2

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5-Hydroxyflavone - ≥98%(HPLC) , CAS No.491-78-1

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