CAS: 2142-73-6; 1-(2,5-Dimethylphenyl)Ethanone

该化合物是一种有机化合物,其特性是氯酮功能组;其特性是2和5位置用两组甲基组替代的苯基环,以及一种异丙酮;该化合物一般是无色的,可粉黄,具有独特的芳香味;在乙醇和乙醚等有机溶剂中可中度溶解,但由于其水分缺乏性,其溶解性有限;该化合物主要用于各种有机化合物的合成和食品工业的调味剂;该化合物的化学结构允许其参与各种反应,包括弗里德尔-氯酸盐酶和其他电动机性替代;安全数据表明,应谨慎处理该化合物,因为它可能会对皮肤和眼睛产生刺激;建议在远离光的冷干地方适当储存,以保持其稳定性并防止降解.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

上下游产品

CAS号106-42-3 对二甲苯 | CAS号75-36-5 乙酰氯 | CAS号108-24-7 乙酸酐 | CAS号50690-11-4 Ethanone, 2-chl... | CAS号75-08-1 乙硫醇 | CAS号7404-77-5 1-(2-hydroxy-2,... | CAS号64-19-7 冰醋酸 | CAS号610-72-0 2,5-二甲基苯甲酸 | CAS号540-63-6 1,2-乙二硫醇 | CAS号32917-52-5 1-(2,5-二甲基苯基)乙醇 | CAS号53882-93-2 2,5-二甲基苯甲酰基乙腈 | CAS号5379-16-8 3,5-二甲基苯乙酮 | CAS号3637-01-2 3,4-二甲基苯乙酮 | CAS号22328-43-4 2,5-二甲基苯甲酰氯 | CAS号23935-13-9 1-Propanone,3-(... | CAS号74331-70-7 2-乙炔-1,4-二甲基苯 | CAS号6051-66-7 2,5-二甲基对苯二甲酸 | CAS号610-72-0 2,5-二甲基苯甲酸 | CAS号3347-99-7 4-甲基间苯二甲酸

合成工艺路线路线简述

    2,5-二甲基苯乙烯置于双氧水,[(2-Me-8-Aq)Pd(Mecn)2](Otf)2体系中,用 水,乙腈 用作溶剂,以72 %的收率获得2,5-二甲基苯乙酮
    参考文献:8-氨基喹啉的水溶性三聚体和单体钯配合物的合成,表征和催化
    标题:8-氨基喹啉的水溶性三聚体和单体钯配合物的合成,表征和催化
    摘要:8-氨基喹啉与乙酸钯等摩尔反应合成了水溶性中性三聚钯配合物.单体和三聚体阳离子钯络合物也已用受控量的三氟甲磺酸合成.配合物已通过 X 射线研究和其他光谱研究进行了表征.已评估中性钯络合物在水介质中将苯甲醇氧化成醛,阳离子钯络合物已评估将苯乙烯氧化成甲基酮.
    Doi:10.1002/ejic.202200559

    海关参考信息

    专利信息


    专利号:US-5426196-A
    优先权日:1993-12-22
    标题 :Synthesis of diaryl methanes
    发明人:FANG FRANCIS G
    权利人:GLAXO INC
    摘要:The present Invention includes synthetic steps and intermediates involved in the following reaction scheme a of converting compounds of Formula (II) to the diarylmethanes of Formula (I): ##STR1## wherein: Y is oxygen or sulfur; n A, B, C, D, and E are carbon or 1, 2 or 3 of A, B, C, D, and E are independently nitrogen, and the others are carbon; and n wherein n R 1 through R 10 are selected independently from the group consisting of: hydrogen, hydroxy, alkyl, C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl alkyl, alkenyl, hydroxy alkyl, alkoxy alkyl, perhalo-alkyl, amino, nitro, nitrile, halo, carboxyl, sulfonyl, acyl, formyl, carbamoyl, trifluoromethyl, aminomethyl, azido, amido, hydrazino, aryl, aryloxy, heteroaryl, or aryl or heteroaryl, mono, di, or tri substituted with one or more hydrogen, hydroxy, alkyl, C 3 -C 8 cycloalkyl, C 3 -C 8 cycloalkyl alkyl, alkenyl, hydroxy alkyl, alkoxy alkyl, perhaloalkyl, amino, nitro, nitrile, halo, carboxyl, sulfonyl, acyl, formyl, carbamoyl, trifluoromethyl, aminomethyl, azido, amido, hydrazino, aryl, aryloxy, or heteroaryl groups and; n the pharmaceutically acceptable salts and solvates thereof.

    专利号:WO-9517408-A1
    优先权日:1993-12-22
    标题 :Synthesis of diaryl methanes

    专利号:US-8664424-B2
    优先权日:2011-03-13
    标 题:Method for preparing 2,5-dimethylphenylacetic acid
    发明人:WANG PING; FAN XIAOBIN; LIN XINGJUN; HE ZHAOHUI
    权利人:WANG PING; FAN XIAOBIN; LIN XINGJUN; HE ZHAOHUI; LIANHE CHEMICAL TECHNOLOGY CO LTD; JIANGSU LIANHE CHEMICAL TECHNOLOGY CO LTD
    摘要:Provided is a method for preparing 2,5-dimethylphenylacetic acid, wherein p-xylene is mixed with paraformaldehyde and concentrated hydrochloric acid in a solvent of ion liquid to obtain 2,5-dimethyl benzyl chloride by the chloromethylation reaction. Then, 2,5-dimethyl benzyl chloride is introduced into a reactor with an acid binding agent and a solvent, the carbonylation and hydrolysis reaction is conducted in the presence of a catalyst to obtain 2,5-dimethylphenylacetic acid. The present process has new route, less synthesis steps, simple operation, lower cost, increased yield, and is friendly to the environment. Therefore, the method is suitable for industrial production.

    专利号:US-8513241-B2
    优先权日:2008-03-28
    标题 :3,4-dihydro-2H-pyrazino[1,2-A]indol-1-one derivatives active as kinase inhibitors, process for their preparation and pharmaceutical compositions comprising them
    发明人:CERVI GIOVANNI; D ANELLO MATTEO; PAPEO GIANLUCA MARIANO ENRICO; SALOM BARBARA
    权利人:CERVI GIOVANNI; D ANELLO MATTEO; PAPEO GIANLUCA MARIANO ENRICO; SALOM BARBARA; NERVIANO MEDICAL SCIENCES SRL
    摘要:Compounds which are 3,4-dihydro-2H-pyrazino[1,2-a]indol-1-one derivatives or pharmaceutically acceptable salts thereof, their preparation process and pharmaceutical compositions comprising them are disclosed; these compounds are useful in the treatment of diseases caused by and/or associated with an altered protein kinase activity such as cancer, viral infection, prevention of AIDS development in HIV-infected individuals, cell proliferative disorders, autoimmune and neurodegenerative disorders; also disclosed is a process under Solid Phase Synthesis conditions for preparing the compounds of the invention and chemical libraries comprising a plurality of them.

    专利号:CN-117568821-A
    优先权日:2023-11-23
    标题:Electrochemical synthesis method of quinoxaline derivative
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    主要参考文献

    参考标题:Synthesis Of Functionalized Vinylsilanes Via Metal-Free Dehydrogenative Silylation Of Enamides
    作者:Xi-Hao Chang,Zi-Lu Wang,Meng Zhao,Chao Yang,Jie-Jun Li,Wei-Wei Ma,Yun-He Xu |发布日期:2020.2.21
    摘要:A Novel Method Of Metal-Free Dehydrogenative Silylation Of Enamides Has Been Developed. The Desired Functionalized Vinylsilane Products Were Obtained In Moderate To Good Yield And With High Stereoselectivities. This Protocol Displays Good Tolerance Of Various Functionalities. Furthermore, The High Chemoselectivity Of This Reaction Enables Us To Introduce Different Unsaturated C-C Moieties To The Products

    合成参考文献


    摘要:Götzinger, A. C.; Müller, T. J. J., Science of Synthesis Knowledge Updates, (2017) 3, 33.
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