CAS: 2040-04-2; 2',6'-Dimethoxyacetophenone

该化合物是一种有机化合物,其特征是氯酮功能组和一个替代芳香环,其特征是:一种具有两种甲氧基(-OCH)替代成分的有机化合物,其位置是2和6个,影响其化学反应和物理特性.该化合物一般是黄色的黄色到浅褐色固体或液体,取决于其纯度和形态.它溶于乙醇和乙醚等有机溶剂,但由于其水分芳香结构,在水溶性中溶解性有限.由于存在甲氧基苯基组,其电子摄取性会增强其电子摄取性,从而可能影响其在电子动力替代反应中的再活动性.此外,1-(2,6-二甲基氧基苯基)乙酮经常用于有机合成,并可能作为各种药品和农用化学品生产的中间体.其安全性特征应当与所有化学物质一起考虑,并应采用适当的处理程序来减少任何潜在危害.

英文名称2',6'-Dimethoxyacetophenone
中文名称1-(2,6-二甲氧基苯基)乙酮
IUPAC名称1-(2,6-dimethoxyphenyl)ethan-1-one
其它别名2',6'-二甲氧基苯乙酮; 2,6-Methoxy Acetophenone
CAS编号2040-04-2
MFCD编号:MFCD00008729
EINECS号:218-034-1
分子式:C10H12O3
分子量:180.2
产品CID: 1034566
产品分类有机原料→分子砌块→芳环类化合物→苯类化合物

相似结构搜索
InChIKey: XEUGKOFTNAYMMX-UHFFFAOYSA-N
InChI=1S/C10H12O3/c1-7(11)10-8(12-2)5-4-6-9(10)13-3/h4-6H,1-3H3…
计算化学: 氢键受体数3.0氢键供体数0.0可旋转键数3.0

MSDS等安全信息

GHS符号GHS07
警示词Warning
危险描述H302-H315-H319-H335
防范说明P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
危险等级IRRITANT
UN编号NONH for all modes of transport
安全声明22-24/25
WGK Germany3

上下游产品

合成工艺路线路线简述

合成目标产物 2',6'-Dimethoxyacetophenone 主要起始原料 2',6'-Dihydroxyacetophenone And Iodomethane
(文献来源)合成步骤主要原料 2',6'-Dihydroxyacetophenone 和 Iodomethane

8-乙酰基-7-羟基-4-甲基-2H-1-苯并吡喃-2-酮置于sodium Hydroxide体系中,化学反应生成2,6-二甲氧基苯乙酮
参考文献:Limaye; Gangal,Rasayanam,1936,Vol. 1,P. 64,66
标题:Limaye; Gangal,Rasayanam,1936,Vol. 1,P. 64,66

海关参考信息

2902600000-乙苯
2905110000-甲醇
2907221000-对苯二酚
2912110000-甲醛
💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
详情请参考：📖 海关编码查询和海关进出口税则

专利信息

专利号:WO-2010001220-A1
优先权日:2008-07-01
标题 :New 1,2,4-triazine derivatives and biological applications thereof
发明人：DESROY NICOLAS; DENIS ALEXIS; GERUSZ VINCENT; OLIVEIRA CHRYSTELLE; VONGSOUTHI VANIDA; MOREAU FRANCOISE; ESCAICH SONIA
权利人:MUTABILIS SA; DESROY NICOLAS; DENIS ALEXIS; GERUSZ VINCENT; OLIVEIRA CHRYSTELLE; VONGSOUTHI VANIDA; MOREAU FRANCOISE; ESCAICH SONIA
摘要:The invention relates to new 1,2,4-triazine derivatives of formula (I): wherein A, B, R2 and Y are defined in the application, their preparation and intermediates, their use as drugs and pharmaceutical compositions and associations containing them. The compounds of formula (I) are capable of inhibiting bacterial heptose synthesis.

专利号:RU-2170230-C2
优先权日:1995-12-08
标题:Novel derivatives of pyrazole, method of their synthesis and pharmaceutical compositions containing thereof

专利号:RU-2195455-C2
优先权日:1995-04-11
标题 :Substituted 1-phenyl-3-carboxamides and their pharmaceutically acceptable salts, method of their synthesis, intermediate compounds and pharmaceutical composition based on thereof showing affinity to human neurotensin receptors