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19492-03-6

19492-03-6 Structure

19492-03-6 Structure
IdentificationBack Directory
[Name]

8-HYDROXY-7-METHOXYCOUMARIN
[CAS]

19492-03-6
[Synonyms]

DAPHNETIN METHYL ETHER
Daphnetin 7-Methyl ethe
DAPHNETIN-7-METHYL ETHER
8-HYDROXY-7-METHOXYCOUMARIN
7-Methoxy-8-hydroxycoumarin
8-hydroxy-7-methoxychromen-2-one
8-Hydroxy-7-methoxy-2H-chromen-2-one
7-Methoxy-8-hydroxy-2H-1-benzopyran-2-one
8-Hydroxy-7-methoxy-2H-1-benzopyran-2-one
2H-1-Benzopyran-2-one, 8-hydroxy-7-methoxy-
8-HYDROXY-7-METHOXYCOUMARIN ISO 9001:2015 REACH
[EINECS(EC#)]

218-290-4
[Molecular Formula]

C10H8O4
[MDL Number]

MFCD00075652
[MOL File]

19492-03-6.mol
[Molecular Weight]

192.17
Chemical PropertiesBack Directory
[Melting point ]

176°C
[Boiling point ]

381.9±42.0 °C(Predicted)
[density ]

1.377
[pka]

7.78±0.20(Predicted)
[BRN ]

168393
[LogP]

0.620 (est)
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[HS Code ]

2932209090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Hydrochloric acid-->Ethyl acetate-->Diethyl ether-->Benzene-->Hexane-->N,N-Diethylaniline-->Ethyl (triphenylphosphoranylidene)acetate-->2,3-Dihydroxy-4-methoxybenzaldehyde
[Preparation Products]

7,8-Dihydroxycoumarin
Hazard InformationBack Directory
[Uses]

8-Hydroxy-7-methoxycoumarin is a phenylpropanoid isolated from the calyxes of Physalis alkekengi L. var. franchetii (Mast.) Makino. 8-Hydroxy-7-methoxycoumarin shows cytotoxicity against GLC4 and COLO 320 cancer cell after continuous incubation (4 days) with IC50s of 179 μM and 145 μM[1][2].
[Definition]

ChEBI: 8-Hydroxy-7-methoxy-2H-1-benzopyran-2-one is a hydroxycoumarin.
[Synthesis]

Preparation of 8-HYDROXY-7-METHOXYCOUMARIN (ryanodine-7-methyl ether) (Ⅱ-aa): weighing 7,8-dihydroxycoumarin 500mg in a three-mouth bottle, adding N,N-dimethylformamide 5mL to dissolve the sample, adding sodium carbonate 850mg, stirring the reaction for 1
[References]

[1] HuiLv, et al. Chemical constituents from the calyxes of Physalis alkekengi L. var. franchetii (Mast.) Makino. Biochemical Systematics and Ecology, Volume 78, June 2018, Pages 63-65.
[2] H Kolodzie, et al. Structure-cytotoxicity relationships of a series of natural and semi-synthetic simple coumarins as assessed in two human tumour cell lines. Z Naturforsch C J Biosci. 1997 Mar-Apr;52(3-4):240-4. DOI:10.1515/znc-1997-3-416
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