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300748

Sigma-Aldrich

2′,6′-Dimethoxyacetophenone

98%

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About This Item

Linear Formula:
(CH3O)2C6H3COCH3
CAS Number:
Molecular Weight:
180.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

bp

135-136 °C/2 mmHg (lit.)

mp

68-70 °C (lit.)

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Facile preparations of 4-fluororesorcinol.
Belanger PC, et al.
Canadian Journal of Chemistry, 66(6), 1479-1482 (1988)
A Bobik et al.
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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