CAS: 86-39-5; 2-Chloro-9H-Thioxanthen-9-One

该化合物是一种有机化合物,被归类为二氧化二氮衍生物,其特点是芳香结构,在二位硫氧烷框架中存在氯原子,通常看起来像黄色至橙色晶状固体,因其光化学特性而闻名,在各种应用中,包括在聚合过程和染色过程中的光化活性剂等,该化合物在水中具有相对较低的溶解性,但在乙醇和丙酮等有机溶剂中具有溶解性,其分子结构中含有氟氧苯乙烯核心,有助于其吸收紫外光的能力,导致在接触光时生成活性物种,在材料科学和光化学领域特别有价值.此外,2-氯甲氧苯丙酮可能具有中度毒性,需要在处理和使用过程中采取适当的安全措施.

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

2-amino-9H-thioxanthen-9-one 3-(Dimethylamino)propyl chloride 2-carboxyphenyl 4-chlorophenyl sulphide Thiosalicylic acid 2-chloro-9-(3-dimethylamino-propyl)-thioxanthen-9-ol sulfure de pentamethylene thioxanthene 2-Chloro-9-(4-tetrahydrothiopyranyl)thioxanthen-9-ol

合成工艺路线路线简述

  • 合成目标产物 2-Chlorothioxanthone 主要起始原料 Nsc54679
  • 6469-85-8 = 86-39-5
    反应条件:1.1 Reagents: Sulfuric Acid; 1 H,100 °C
    标题:Catalyst-Controlled Stereoselective Barton-Kellogg Olefination
    作者:Schmidt,Tanno A.; Et Al
    参考文献:Angewandte Chemie 日期:2021 卷标:60(44) 页码:23911-23916]

    22096-70-4 = 86-39-5
    反应条件:1.1 Reagents: Potassium Hydroxide Solvents: Methanol; Rt; 1 H,80 °C; 80 °C -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water1.3 Reagents: Sulfuric Acid; Rt; 12 H,100 °C; 100 °C -> Rt1.4 Reagents: Sodium Bicarbonate Solvents: Water
    标题:A Mild And Facile Synthesis Of Aryl And Alkenyl Sulfides Via Copper-Catalyzed Deborylthiolation Of Organoborons With Thiosulfonates
    作者:Yoshida,Suguru; Et Al
    参考文献:Chemical Communications (Cambridge 日期:2015 卷标:51(93) 页码:16613-16616]

    113-59-7 = 86-39-5
    反应条件:1.1 Reagents: Oxygen Catalysts: N-Hydroxysuccinimide,1,3,5-Triazine-2,4,6-Triamine Homopolymer Solvents: Acetonitrile; 16 - 40 H,Rt
    标题:A Metal-Free Heterogeneous Photocatalyst For The Selective Oxidative Cleavage Of C=c Bonds In Aryl Olefins Via Harvesting Direct Solar Energy
    作者:Zhang,Yu; Et Al
    参考文献:Green Chemistry 日期:2020 卷标:22(14) 页码:4516-4522]

    107572-07-6 = 86-39-5
    反应条件:1.1 Reagents: Pyridine Catalysts: Cobalt,Bis[[2,3-Butanedione Di(Oximato-Kn)](1-)]Chloro(Pyridine)-,(Oc-6-42)- Solvents: Dichloromethane; 24 H,Rt
    标题:Direct Excitation Of Aldehyde To Activate The C(Sp2)-H Bond By Cobaloxime Catalysis Toward Fluorenones Synthesis With Hydrogen Evolution
    作者:Guo,Jia-Dong; Et Al
    参考文献:Angewandte Chemie 日期:2023 卷标:62(7)]

    73129-22-3 = 86-39-5 [标题:Reaction Conditions
    标题:Neurotropic And Psychotropic Agents. Clxviii. Tricyclic Psychotropic Agents Containing Two Chalcogen Atoms In The Central Ring: 8-Substituted 6-(4-Piperidyl)-6H-Dibenz[b,E]-1,4-Oxathiepins
    作者:Sindelar,Karel; Et Al
    参考文献:Collection Of Czechoslovak Chemical Communications 日期:1982 卷标:47(11) 页码:3077-93]

    446-52-6 = 86-39-5
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Dimethylformamide; 150 °C2.1 Reagents: Pyridine Catalysts: Cobalt,Bis[[2,3-Butanedione Di(Oximato-Kn)](1-)]Chloro(Pyridine)-,(Oc-6-42)- Solvents: Dichloromethane; 24 H,Rt
    标题:Direct Excitation Of Aldehyde To Activate The C(Sp2)-H Bond By Cobaloxime Catalysis Toward Fluorenones Synthesis With Hydrogen Evolution
    作者:Guo,Jia-Dong; Et Al
    参考文献:Angewandte Chemie 日期:2023 卷标:62(7)]

    92-38-6 = 86-39-5
    反应条件:1.1 Reagents: Oxygen Catalysts: Acetic Acid,2,3-Dichloro-5,6-Dicyano-1,4-Benzoquinone,Tert-Butyl Nitrite Solvents: 1,2-Dichloroethane; 12 H,Rt
    标题:Visible-Light-Induced Aerobic Oxidation Of Benzylic C(Sp 3 )-H Of Alkylarenes Promoted By Ddq,Tert -Butyl Nitrite,And Acetic Acid
    作者:Pan,Decheng; Et Al
    参考文献:Synlett 日期:2019 卷标:30(2) 页码:218-224]

    1449571-63-4 = 86-39-5
    反应条件:1.1 Reagents: Disodium Sulfide Solvents: Dimethylformamide; 1 H,60 °C
    标题:A Convenient Synthesis Of 9H-Thioxanthen-9-Ones And Their Aza-Analogs
    作者:Kobayashi,Kazuhiro; Et Al
    参考文献:Heterocycles 日期:2013 卷标:87(12) 页码:2577-2587]

    6469-93-8 = 86-39-5
    反应条件:1.1 Reagents: 3,5-Dinitrobenzotrifluoride,1,1,1,3,3,3-Hexafluoro-2-Propanol Solvents: Dichloromethane; 24 H,-30 °C1.2 Reagents: Formaldehyde Solvents: Acetonitrile,Water; -30 °C; 16 H,Rt1.3 Reagents: Dipotassium Phosphate; 20 H
    标题:Photoexcited Nitroarenes For The Oxidative Cleavage Of Alkenes
    作者:Ruffoni,Alessandro; Et Al
    参考文献:Nature (London 日期:2022 卷标:610(7930) 页码:81-86]

    41932-38-1 = 86-39-5
    反应条件:1.1 Reagents: Hexadecyltrimethylammonium Bromide,Oxygen Catalysts: Bismuth Tungsten Oxide (Bi2Wo6) Solvents: Water; 24 H,Rt
    标题:Rapid Microwave Synthesis Of Bi2Wo6 For C=c Bonds Oxidative Cleavage To Ketones With Visible Light Irradiation In Aerobic Micellar Medium
    作者:Liu,Tianxiang; Et Al
    参考文献:Journal Of Catalysis 日期:2023 卷标:417 页码:41-51]

    1229-38-5 = 86-39-5
    反应条件:1.1 Reagents: Permanganic Acid (Hmno4),Potassium Salt (1:1)
    标题:Selective Oxidation Of Thioxanthene Derivatives
    作者:Tammilehto,Seija; Et Al
    参考文献:Acta Pharmaceutica Suecica 日期:1986 卷标:23(5) 页码:289-94]

    119-80-2 = 86-39-5
    反应条件:1.1 Catalysts: Sulfuric Acid Solvents: Water; Rt; 4 H,Cooled1.2 Reagents: Water
    标题:Synthesis Of Thiaxanthone Derivatives
    作者:Mao,Xue-Feng; Et Al
    参考文献:Huaxue Shiji 日期:2008 卷标:30(12) 页码:932-934]

    88-65-3 = 86-39-5
    反应条件:1.1 Reagents: Potassium Carbonate Catalysts: Copper Solvents: Dimethylformamide; Overnight,Rt -> Reflux; Reflux -> Rt1.2 Reagents: Hydrochloric Acid Solvents: Water; Acidified,Cooled2.1 Reagents: Sulfuric Acid; 1 H,100 °C
    标题:Catalyst-Controlled Stereoselective Barton-Kellogg Olefination
    作者:Schmidt,Tanno A.; Et Al
    参考文献:Angewandte Chemie 日期:2021 卷标:60(44) 页码:23911-23916
1,4-二氯苯置于lithium Hydroxide Monohydrate,硫酸,硫化氢,Sodium Hydroxide体系中,用 甲苯 作为反应溶剂,化学反应 15.0H,反应生成 2-氯噻吨酮
参考文献:一种氯代硫蒽酮的合成新方法
标题:一种氯代硫蒽酮的合成新方法
摘要:本发明公开了一种氯代硫蒽酮的合成新方法,属于化工技术领域.该方法包括如下步骤:首先将硫氢化钠溶液加入到硫化氢发生器中,再向硫化氢发生器中滴加酸,产生的气体被导入至预热后的管道反应器中;然后向管道反应器中泵入预热后的对二氯苯,对二氯苯与硫化氢气体发生反应,将反应产物冷却后得到液体和气体,液体经精馏提纯得巯基氯苯;其次,向烧瓶中加入反应溶剂和碱,搅拌,再加入巯基氯苯和邻氯苯甲酸进行回流反应,反应结束后经后处理得中间体2‑羧基‑4'‑氯二苯硫醚;最后将2‑羧基‑4'‑氯二苯硫醚加入至浓硫酸中进行分子内环合脱水反应,反应结束后经提纯得目标产品.本发明方法操作简便,反应条件温和,清洁环保,产品收率和纯度高.

海关参考信息

专利信息


专利号:US-9969823-B1
优先权日:2011-09-01
标题 :Synthesis and polymerization of vinyl triazolium ionic liquids
发明人:LUEBKE DAVID; NULWALA HUNAID; MATYJASZEWSKI KRZYSZTOF; ADZIMA BRIAN
权利人:US ENERGY; THE US DEPARTMENT OF ENERGY
摘要:Herein, we describe polymerized ionic liquids, demonstrate the synthesis of polymerized ionic liquids, and demonstrate the polymerization of triazolium monomers. One embodiment shows the polymeriazation of the triazolium monomers with bis(trifluoromethanesulfonyl)imide anions. In another embodiment we show the feasibility of copolymerizing with commodity monomers such as styrene using free radical polymerization techniques.

专利号:EP-4428168-A1
优先权日:2023-03-08
标 题 :Polyurethane/oligomeric urethane synthesis method by radiation
发明人:AKBULUT HÜSEYIN; ÇEL KBA SENA; ENADA SEHER; U AKLI MÜGE; DEM RBAY DUYGU
权利人:CHT TURKEY KIMYA SANAYI VE TICARET A S
摘要:In particular, the invention relates to the synthesis of radiation-curable polyurethane/oligomeric urethane dispersions of anionic and cationic characters, containing neutralization techniques characterized by the selection of counter ions as monomers and/or agents which can be polymers acting as promoters under radiation, to a radiation polyurethane/oligomeric urethane synthesis method that enables the creation of radiation curable binder systems without using cosolvents, surfactants, emulsifiers, defoamers, stabilizers and additives, wherein all components of the radiation-curable binder systems can be polymerized.

专利号:US-6031014-A
优先权日:1998-12-08
标题:Initiator compositions and methods for their synthesis and use
发明人:CRIVELLO JAMES V
摘要:Cationic polymerization initiators of formula ##STR1## are disclosed. The acyl sulfonium salts of the present invention differ from known acyl sulfonium initiators in that the substituents R 2 and R 3 on the sulfur are larger and more complex than the lower alkyl and lower alkylene of known photoinitiators. Processes for the synthesis of the novel acyl sulfonium salts and prepolymer compositions containing them are also disclosed.

专利号:US-9175026-B2
优先权日:2011-03-23
标题:Synthesis of thioether containing trialkoxysilanes
发明人:GARRELL ROBIN L; TUCKER-SCHWARTZ ALEXANDER K
权利人:GARRELL ROBIN L; TUCKER-SCHWARTZ ALEXANDER K; UNIV CALIFORNIA
摘要:The invention relates to a radical-initiated thiol-ene or thiol-yne “clickâ€? reaction that provides a simple and efficient route to diverse trialkoxysilanes. Trialkoxysilanes made in this way are obtained in quantitative to near-quantitative yields with high purity without any or minimal purification. A wide range of functional groups is tolerated in this approach, and even complex alkenes click with the silane precursors. The modular nature of these radical-based thiol-ene or thiol-yne “clickâ€? reactions allows a wide variety of pendant groups to be coupled to silane compounds that can then be coupled to a wide variety surfaces in order to modify their material properties. Consequently, such radical initiated thiol-ene and thiol-yne reactions provide facile and efficient methods for preparing an enormous number of surface-active functional trialkoxysilanes.

专利号:US-8475998-B2
优先权日:2010-12-20
标 题 :Compound synthesis method, microarray, acid-transfer composition, and biochip composition
发明人:YUN HYOJIN; YOO CHANGEUN; KIM MYUNG-SUN; KIM SOO-KYUNG; NISHIKAWA KOUJI; GOTO HIROFUMI; MIYAMOTO HIDETOSHI
权利人:YUN HYOJIN; YOO CHANGEUN; KIM MYUNG-SUN; KIM SOO-KYUNG; NISHIKAWA KOUJI; GOTO HIROFUMI; MIYAMOTO HIDETOSHI; SAMSUNG ELECTRONICS CO LTD; JSR CORP
摘要:A compound synthesis method includes bonding a first compound to a substrate to form a first film. A second film is formed on the first film using an acid-transfer composition including (A) a polymer that includes a structural unit shown by a following formula (1) and a structural unit shown by a following formula (2), (B) a photoacid generator shown by a following formula (3), and (C) a sensitizer shown by a following formula (4). The second film is exposed to remove the protecting group from the first compound under an exposed area of the second film. An acid generated in the exposed area of the second film is transferred to the first film. The second film after being exposed is removed. A second compound is bonded to the first compound from which the protecting group has been removed.

专利号:US-2005170281-A1
优先权日:2002-06-21
标题:Method of cleaving labile functional groups from chemical compounds
发明人:STENGELE KLAUS-PETER
摘要:The present invention provides a method of cleaving labile functional groups from molecules by exposure to electromagnetic radiation in which the molecules are contacted with a chemical compound whose triplet state is energetically higher than the triplet state of the labile functional group and are then exposed to electromagnetic radiation, with the labile functional group and the suitable chemical compound having different absorption maxima for electromagnetic radiation. Further, the invention provides a method of manufacturing DNA chips by spatially addressed, light-controlled nucleotide synthesis on solid substrates. In addition, the present invention provides a chemical composition comprising a molecule with a labile functional group and a chemical compound whose triplet state is higher than the triplet state of the labile functional group, with the labile functional group and the chemical compound having different absorption maxima for electromagnetic radiation, and describes the use of the chemical composition in the manufacture of DNA chips.
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主要参考文献

[参考文献]: J E Pettersen, Et Al. Identification Of 2-Chlorothioxanthen-9-One In Gastric Aspirate In A Case Of Chlorprothixene Poisoning. J Pharm Sci. 1981 Jul;70(7):812-3.

合成参考文献


摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
摘要:Rudorf, W.-D., Science of Synthesis, (2003) 14, 765.
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