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300748

2′,6′-Dimethoxyacetophenone

Name: 2′,6′-Dimethoxyacetophenone
Brand: ALDRICH

98%

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About This Item

Linear Formula:

(CH₃O)₂C₆H₃COCH₃

CAS Number:

2040-04-2

Molecular Weight:

180.20

NACRES:

NA.22

PubChem Substance ID:

24857937

UNSPSC Code:

12352100

EC Number:

218-034-1

MDL number:

MFCD00008729

Assay:

98%

Form:

solid

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Properties

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

Description

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

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Inhibitors of hepatic mixed function oxidases. I. The metabolism of 2,6-dihydroxy-,2-hydroxy-6-methoxy- and 2,6-dimethoxyacetophenones.

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.

Facile preparations of 4-fluororesorcinol.

Belanger PC, et al.

Canadian Journal of Chemistry, 66(6), 1479-1482 (1988)

Global Trade Item Number

SKU	GTIN
300748-5G	04061826659410