CAS: 14933-76-7; 3-Ethyl-2-Methylbenzo[d]Thiazol-3-Ium 4-Methylbenzenesulfonate

该化合物是一种有机化合物,其结构特征包括苯并氮基和磺酸组,该化合物一般是一种固体或晶状物质,由于全氟辛烷磺酸组的存在而溶于水和酒精等极地溶剂中,这增加了其离子特性;苯并二甲基苯甲醚环有其芳香特性,有可能传播荧光或其他电子特性;它经常用于各种用途,包括染色或合成其他化学化合物;在苯并聚环上存在乙基和甲基替代成分会影响其再活动及与其他分子的相互作用;在处理和毒性信息时,应参考安全数据表,如任何化学物质.

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合成工艺路线路线简述

    📜2-甲基苯并噻唑,对甲苯磺酸乙酯 反应生成3-乙基-2-甲基苯并唑对甲基苯磺酸酯
    参考文献:Photophysics Of Cyanine Dyes On Surfaces: Laser-Induced Photoisomer Emission Of 3,3'-Dialkylthiacarbocyanines Adsorbed On Microcrystalline Cellulose
    标题:Photophysics Of Cyanine Dyes On Surfaces: Laser-Induced Photoisomer Emission Of 3,3'-Dialkylthiacarbocyanines Adsorbed On Microcrystalline Cellulose
    摘要:三种硫代碳青霉素染料,3,3'-二甲基硫代碳青霉素碘化物(dmtcc),3,3'-二乙基硫代碳青霉素碘化物(detcc)和3,3'-二丙基硫代碳青霉素碘化物(dptcc)在微晶纤维素上的光物理学研究,浓度范围为5.0.10-4至10.0 μmol G-1.使用基态漫反射吸收技术,仅检测到所有探针的h聚集物形成.形成的聚集物量取决于样品的水合度,始终随着样品干燥而减少.所有吸附染料的荧光量子产率比在非粘性溶剂中观测到的高一个数量级,Dmtcc为0.98,Detcc为0.96,Dptcc为0.63.记录了激光诱导的荧光发射(使用增强电荷耦合器件检测系统),作为激光功率的函数,结果显示对于受高激光强度照射的干燥浓缩样品,检测到了第二个荧光发射带(相对于单体发射的巴托克移位).这种发射显示对激光功率的超线性依赖.这里检测到的新发射来自通过单体的荧光异构体形成的,通过双光子吸收过程.
    Doi:10.1135/cccc19990459

    海关参考信息

    专利信息


    专利号:US-3943142-A
    优先权日:1969-01-24
    标 题:Dye intermediates and their preparation and use in the synthesis of methine dyes
    发明人:OWEN JOHN R
    权利人:EASTMAN KODAK CO
    摘要:Compositions of matter are provided comprising a stable, non-vaporous monomeric methylene base selected from a 2-methylenethiazoline; a 2-methylenebenzothiazoline; a 2-methylenenaphthothiazoline; a 2-methylenebenzoselenazoline; and a 2-methylenenaphthoselenazoline. The compositions of the invention are prepared by reacting the parent 2-methyl quaternary salt with a non-hydroxylic base which removes a proton of the heterocyclic salt together with a proton acceptor which inhibits build-up of the hydro salt of the non-hydroxylic base, the reaction being conducted under anhydrous conditions in a non-hydroxylic liquid in which the heterocyclic quaternary salt is sufficiently insoluble to inhibit dimer formation. The compositions of the invention are employed in the preparation of methine dyes.

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    合成参考文献


    参考文献:10.1007/bf00473090
    摘要:Sych ED, Fesenko IV. Condensation of 1,3-thiazan-2,4-dithione. Chemistry of Heterocyclic Compounds. 1971 Feb;7(2):210–1. doi: 10.1007/bf00473090.
    参考文献:10.1007/bf00472307|10.1007/bf00474775
    摘要:Sych ED, Moreiko OV. Thiazolocyanines. Chemistry of Heterocyclic Compounds. 1973 Sep;9(9):1078–81. doi: 10.1007/bf00474775.
    参考文献:10.1007/bf00471830
    摘要:Kazymov AV, Shchelkina EP. Reaction of acetoacetaldehyde tetraethylacetal with quaternary salts of heterocyclic bases and some reactions of the products. Chemistry of Heterocyclic Compounds. 1972 Dec;8(12):1464–7. doi: 10.1007/bf00471830.
    参考文献:10.1007/bf00633182
    摘要:Amosova SV, Nikol'skaya AN, Belogorlova NA, Gendin DV, Kashik TV, Larin MF. Halogen-containing spiro compounds based on a 4-vinyloxyethyl-1,4-perhydrothiazine 1-oxide. Chemistry of Heterocyclic Compounds. 1988 Jul;24(7):810–2. doi: 10.1007/bf00633182.
    参考文献:10.1007/bf00473089
    摘要:Sych ED, Gorb LT. Some reactions of 2-methyl-3-ethoxycarbonyl-1,4,5,6-tetrahydropyridine-6-thione. Chemistry of Heterocyclic Compounds. 1971 Feb;7(2):207–9. doi: 10.1007/bf00473089.
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