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assay
98%
form
solid
bp
135-136 °C/2 mmHg (lit.)
mp
68-70 °C (lit.)
functional group
ketone
SMILES string
COc1cccc(OC)c1C(C)=O
InChI
1S/C10H12O3/c1-7(11)10-8(12-2)5-4-6-9(10)13-3/h4-6H,1-3H3
InChI key
XEUGKOFTNAYMMX-UHFFFAOYSA-N
General description
2,6-Dihydroxyacetophenone, its mono- and di-methyl ethers are inhibitors of hepatic mixed function oxidases. Metabolism of 2′,6′-dimethoxyacetophenone was studied.
Application
2′,6′-Dimethoxyacetophenone was used in preparation of 4-fluororesorcinol.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Facile preparations of 4-fluororesorcinol.
Canadian Journal of Chemistry, 66(6), 1479-1482 (1988)
Xenobiotica; the fate of foreign compounds in biological systems, 5(2), 65-72 (1975-02-01)
1. 2,6-Dihydroxyacetophenone, its mono- and di-methyl ethers are inhibitors of hepatic mixed function oxidases. The dimethyl ether is a competitive inhibitor of aminopyrine demethylase with the others displaying mixed kinetics. The metabolism of all three ketones has been studied. 2.
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