ChemicalBook--->CAS DataBase List--->6601-66-7

6601-66-7

6601-66-7 Structure

6601-66-7 Structure
IdentificationBack Directory
[Name]

5,7,8,4''-TETRAMETHOXYFLAVONE
[CAS]

6601-66-7
[Synonyms]

8-Tetramethoxyflavone
5,7,8-trimethoxy-2-(4-methoxyphenyl)chromen-4-one
5,7,8,4'- tetramethoxyflavone 6-Demethoxytangeretin
4H-1-Benzopyran-4-one, 5,7,8-trimethoxy-2-(4-methoxyphenyl)-
[Molecular Formula]

C19H18O6
[MDL Number]

MFCD03427696
[MOL File]

6601-66-7.mol
[Molecular Weight]

342.34
Chemical PropertiesBack Directory
[Melting point ]

216-217℃ (methanol )
[Boiling point ]

536.9±50.0 °C(Predicted)
[density ]

1.243±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard InformationBack Directory
[Chemical Properties]

Pale yellow crystalline powder, soluble in organic solvents such as methanol, ethanol, and DMSO, derived from Citrus aurantium.
[Uses]

6-Demethoxytangeretin is a flavonoid compound that can be isolated from Citrus reticulata. 6-Demethoxytangeretin has anti-inflammatory and anti-allergic activities and can inhibit the production of IL-6 and the expression of related genes in human mast cells through the ALK and MAPK pathways. 6-Demethoxytangeretin can promote CRE-mediated transcription in hippocampal neurons[1][2].
[References]

[1] Kim YM, et al. A citrus flavonoid, 6-demethoxytangeretin, suppresses production and gene expression of interleukin-6 in human mast cell-1 via anaplastic lymphoma kinase and mitogen-activated protein kinase pathways. Biol Pharm Bull. 2014;37(5):871-6. Epub 2014 Feb 5. DOI:10.1248/bpb.b13-00875
[2] Kawahata I, et al. Potent activity of nobiletin-rich Citrus reticulata peel extract to facilitate cAMP/PKA/ERK/CREB signaling associated with learning and memory in cultured hippocampal neurons: identification of the substances responsible for the pharmacological action. J Neural Transm (Vienna). 2013 Oct;120(10):1397-409. DOI:10.1007/s00702-013-1025-x
Spectrum DetailBack Directory
[Spectrum Detail]

5,7,8,4''-TETRAMETHOXYFLAVONE(6601-66-7)1HNMR
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