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Merck
CN

300748

2′,6′-二甲氧基苯乙酮

98%

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关于此项目

线性分子式:
(CH3O)2C6H3COCH3
化学文摘社编号:
分子量:
180.20
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
218-034-1
MDL number:
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产品名称

2′,6′-二甲氧基苯乙酮, 98%

form

solid

SMILES string

COc1cccc(OC)c1C(C)=O

InChI key

XEUGKOFTNAYMMX-UHFFFAOYSA-N

InChI

1S/C10H12O3/c1-7(11)10-8(12-2)5-4-6-9(10)13-3/h4-6H,1-3H3

assay

98%

bp

135-136 °C/2 mmHg (lit.)

mp

68-70 °C (lit.)

functional group

ketone

Application

2′,6′-Dimethoxyacetophenone was used in preparation of 4-fluororesorcinol.

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.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)

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