CAS: 832-53-1; Pentafluorobenzenesulfonyl Chloride

该化合物是一个高度氟化的芳基磺酸氯化物,该化合物的特点是用五氟原子和全氟氯化物组组成的苯环替换,使其成为一种强大的电极,其结构有助于其高度的再活性,特别是在可以用作磺酰剂的核生殖替代反应中;多种氟原子的存在增强了其稳定性和亲脂性,同时也具有独特的电子特性,能够影响其再活动及与其他化学物种的相互作用;该化合物通常用于有机合成,特别是在制作磺酰胺和其他氟化合物时;由于它具有再活性和存在氯,因此应当谨慎地处理,因为它可以是腐蚀性的,可能对接触造成健康危害;适当的安全措施,包括使用个人防护设备和在烟雾罩中工作,在与该物质合作时至关重要.

结构式图片

欧盟法规

ECHA物质ECHA物质C&L通报REACH预注册

上下游产品

CAS号363-72-4 五氟苯 | CAS号879-06-1 3-indole acetamide | CAS号27918-31-6 五氟苯磺酰氯 | CAS号7722-84-1 过氧化氢 | CAS号344-07-0 氯五氟苯 | CAS号771-62-0 五氟硫酚 | CAS号7782-50-5 氯气 | CAS号64-19-7 冰醋酸 | CAS号195533-53-0 Batabulin | CAS号434-90-2 全氟联苯 | CAS号793-73-7 pentafluorophen... | CAS号142-04-1 苯胺盐酸盐 | CAS号344-07-0 氯五氟苯 | CAS号363-72-4 五氟苯 | CAS号711-55-7 1,2,3,4-tetrafl... | CAS号108-20-3 异丙醚 | CAS号784-14-5 2,3,4,5,6-五氟联苯 | CAS号4400-84-4 2,3,4,5,6-penta...

合成工艺路线路线简述

  • 344-07-0 = 832-53-1
    反应条件:1.1 Reagents: Magnesium Solvents: Tetrahydrofuran; -20 °C2.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C; 0 °C
    标题:Chloropentafluorobenzene
    作者:Anilkumar,R.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2005 卷标:1 页码:1-5]

    879-06-1 = 832-53-1
    反应条件:1.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C -> 0 °C
    标题:1-Chloro-2,3,4,5,6-Pentafluorobenzene (Cpfb)
    作者:Anilkumar,R.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2001]

    363-72-4 = 832-53-1
    反应条件:1.1 Reagents: Chlorosulfonic Acid; 3 H,150 °C
    标题:Development Of Hdac Inhibitors Exhibiting Therapeutic Potential In T-Cell Prolymphocytic Leukemia
    作者:Toutah,Krimo; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2021 卷标:64(12) 页码:8486-8509]

    778-36-9 = 832-53-1
    反应条件:1.1 Reagents: Thionyl Chloride
    标题:Sulfur-Nitrogen Compounds. Vii. Preparation And Reactions Of Some Perfluoro Aromatic Sulfur-Nitrogen Compounds
    作者:Glander,I.; Et Al
    参考文献:Journal Of Fluorine Chemistry 日期:1979 卷标:14(5) 页码:403-20]

    1306747-56-7 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7
    反应条件:1.1 25 H,145 - 155 °C2.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt
    标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides
    作者:Bredikhin,Roman A.; Et Al
    参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011]

    344-07-0 = 832-53-1
    反应条件:1.1 Reagents: Magnesium,Sulfur Dioxide Solvents: Tetrahydrofuran1.2 Reagents: Chlorine Solvents: Tetrahydrofuran
    标题:Perfluoro- And Polyfluorosulfonic Acids. Part 22. Polyfluorophenyl Pentafluorobenzenesulfonates And Their Electron-Transfer Reaction With Sodium Iodide
    作者:Chen,Qing Yun; Et Al
    参考文献:Journal Of The Chemical Society 日期:1991 卷标:(7) 页码:1071-5]

    879-06-1 = 832-53-1
    反应条件:1.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C; 0 °C
    标题:Chloropentafluorobenzene
    作者:Anilkumar,R.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2005 卷标:1 页码:1-5]

    = 832-53-1
    反应条件:1.1 Reagents: Potassium Fluoride2.1 Reagents: Magnesium Solvents: Tetrahydrofuran; -20 °C3.1 Reagents: Sulfur Dioxide,Chlorine Solvents: Tetrahydrofuran; -78 °C; 0 °C
    标题:Chloropentafluorobenzene
    作者:Anilkumar,R.; Et Al
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2005 卷标:1 页码:1-5]

    140200-30-2 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7
    反应条件:1.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt
    标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides
    作者:Bredikhin,Roman A.; Et Al
    参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011]

    776-09-0 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7
    反应条件:1.1 Reagents: Sodium Bromide Solvents: Acetonitrile; Rt; 19 H,Rt2.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt
    标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides
    作者:Bredikhin,Roman A.; Et Al
    参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011]

    832-53-1 = 832-53-1 + 344-07-0 + 363-72-4 + 344-04-7
    反应条件:1.1 Catalysts: Cuprous Iodide; 3 H,149 - 154 °C2.1 25 H,145 - 155 °C3.1 Reagents: Sodium Chloride Solvents: Acetonitrile; Rt; 22 H,Rt
    标题:Transformations Of Polyfluoroarenesulfonyl Halides With Alkenes,Polyfluoroarenethiols And Alkali Metal Halides
    作者:Bredikhin,Roman A.; Et Al
    参考文献:International Electronic Conference On Synthetic Organic Chemistry 日期:2011
氯五氟苯置于氯磺酸体系中,用 Neat (No Solvent) 作为反应溶剂,化学反应生成 2,3,4,5,6-五氟苯磺酰氯
参考文献:Development Of Hdac Inhibitors Exhibiting Therapeutic Potential In T-Cell Prolymphocytic Leukemia
标题:Development Of Hdac Inhibitors Exhibiting Therapeutic Potential In T-Cell Prolymphocytic Leukemia
摘要:
DOI:10.1021/acs.Jmedchem.1C00420

专利信息


专利号:EP-0364340-B1
优先权日:1988-10-05
标题:Method for the synthesis of sulfonyl imides
摘要:Method for the synthesis of sulfonylimidides having the formula M((RSO2)2N)y, whrein M is a metal or an ammonium radical quaternary or not, the Rs, which may be identical or similar are organic monovalent radicals, particularly hydrocarbyles and preferably perfluorohydrocarbyles, in C1 to C12, and y is the valence of M. On the one hand, a silazane component selected amongst the silazane compounds M(((R2)3Si)2N)y or the associations of a silazane derivative A((R2)3Si)2N or a fluoride M1Fz of low cross-linking energy is reacted with, on the other hand, at least one sulfonic halogenite component consisting of a sulfonyl fluoride RSO2F or in the association of a sulfonyl chloride RSO2Cl with a fluoride M1Fz, M, R and y having the above-mentionned significations, M1 being selected amongst the Ms and being optionally identical to M, z being the valence of M1 and R2 representing an alkyl in C1 to C4. The imidides obtained for which the R2 are perfluorated radicals and M is an alkaline metal such as Li are usable in association with polyethers for the production of materials of the ionic conduction type for all solid generators in thin films.

专利号:US-5256821-A
优先权日:1988-10-05
标题:Method of synthesis of sulphonylimides
发明人:ARMAND MICHEL B
权利人:ELF AQUITAINE; HYDRO QUEBEC
摘要:Method for the synthesis of sulfonylimidides having the formula M((RSO 2 ) 2 N) y , wherein M is a metal or an ammonium radical quaternary or not, the Rs, which may be identical or similar are organic monovalent radicals, particularly hydrocarbyles and preferably perfluorohydrocarbyles, in C 1 to C 12 , and y is the valence of M. On the one hand, silazane component selected amongst the silazane compounds M(((R 2 ) 3 Si) 2 N) y or the associations of a silazane derivative A((R 2 ) 3 Si) 2 N or a fluoride M 1 F z of low cross-linking energy is reacted with, on the other hand, at least one sulfonic halogenite component consisting of a sulfonyl fluoride RSO 2 F or in the association of a sulfonyl chloride RSO 2 Cl with a fluoride M 1 F z , M, R and y having the above-mentioned significations, M being selected amongst the Ms and being optionally identical to M, z being the valence of M 1 and R 2 representing an alkyl in C 1 to C 4 . The imidides obtained for which the R 2 are perfluorated radicals and M is an alkaline metal such as Li are usable in association with polyethers for the production of materials of the ionic conduction type for all solid generators in thin films.

专利号:US-2010150835-A1
优先权日:2007-02-27
标题:Synthesis of [18F] Fluoromethyl Benzene Using Benzyl Pentafluorobenzenesulfonate
发明人:LANGSTROM BENGT; KARIMI FARHAD; BLOM ELISABETH
权利人:LANGSTROM BENGT; KARIMI FARHAD; BLOM ELISABETH
摘要:The present invention discloses the reactivity of ponytail (“PTâ€?) sulfonates as leaving groups in nucleophilic fluorination reactions. The results showed that using a pentafluorobenzenesulfonate precursor is a suitable leaving group for n. c. a. nucleophilic 18 F-fluorination in synthesis of [ 18 F]fluoromethyl benzene, wherein this is a suitable leaving group for 18F-labeling with moderate reactivity. The PT-precursor seems to be quite stable. In an attempt to purify the crude 18F-labeled product using fluorous solid phase extraction (F-SPE), the radio labeled impurities decreased significantly. This provides an opportunity for utilizing PT methodology in both simple and fast purification methods.

专利号:US-5214218-A
优先权日:1992-05-04
标题 :One step synthesis of methyl t-butyl ether from t-butanol using haloacid-modified clay catalysts
发明人:KNIFTON JOHN F
权利人:TEXACO CHEMICAL
摘要:A method is disclosed wherein t-butanol is reacted with methanol in a reaction zone in one step to provide methyl tert-butyl ether and the improvement of accomplishing the reaction which comprises: n a. Using a catalyst comprising a montmorillonite clay treated with a haloacid; n b. continuously contacting said t-butanol and methanol in a molar amount of about 0.1 to 10 moles of methanol per mole of t-butanol with said catalyst at a temperature of about 20° C. to about 250° C. and a pressure of about atmospheric to about 1000 psig to obtain the methyl tert-butyl ether product.

专利号:EP-2883866-A1
优先权日:2012-08-13
标题 :INTERMEDIATE FOR SYNTHESIS OF 1-(2-DEOXY-2-FLUORO-4-THIO-beta-D-ARABINOFURANOSYL) CYTOSINE, INTERMEDIATE FOR SYNTHESIS OF THIONUCLEOSIDE, AND METHODS FOR PRODUCING THESE INTERMEDIATES

专利号:WO-2014027658-A1
优先权日:2012-08-13
标题 :INTERMEDIATE FOR SYNTHESIS OF 1-(2-DEOXY-2-FLUORO-4-THIO-β-D-ARABINOFURANOSYL) CYTOSINE, INTERMEDIATE FOR SYNTHESIS OF THIONUCLEOSIDE, AND METHODS FOR PRODUCING THESE INTERMEDIATES
科邦特化工(杭州)有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.capot.cn
企业联系电话:0571-85586718👤
📞科邦特化工(杭州)有限公司 ⚠️参考联系方式
联系人:景先生
电话:0571-85586718
手机:13336094967(外贸专线);13336195806(内需专线)
传真:0571-85864795
邮箱:sales@capot.com
通信地址: 浙江省杭州市滨江区江陵路88号万轮科技园
邮编: 310051
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:浙江省杭州市滨江区江陵路88号万轮科技园
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
北京嘉盛扬医药科技有限公司
⚠️ 未注册 · 未认证企业
⚠️ 该商家尚未完成注册及企业认证,请用户仔细辨别,谨慎交易。
数据来源于公开网络搜索,平台未作核实,请自行辨别。
🏢敬请 企业认领
🏬开设公司展台
📢获取免费会员权益
🎖️点亮专属注册企业标签
📇展现公司完整信息 样本查看立即注册认领 →
网址: http://www.chemsun.cn
企业联系电话:010-63786746,63786429,63787357👤
📞北京嘉盛扬医药科技有限公司 ⚠️参考联系方式
联系人:费先生
电话:010-63786746,63786429,63787357
手机:13911777236
传真:010-63787446
邮箱:market@chemsun.cn
通信地址: 北京市丰台科技园海鹰路9号2号楼2层
邮编: 100070
🆔 联系时候可告知是从"百琢研"平台获取的信息.
⚠️ 声明: 该企业未认证、未认领,请自行辨别信息的真实性和可靠性。咨询或交易时请注意风险评估与信息核实,百琢研不参与任何交易。企业认领注册入口→

地址:北京市丰台科技园海鹰路9号2号楼2层
⚠️ 未注册 · 未认证企业
注册入口 备注: 📌 数据来源说明:本展台内容基于各搜索引擎等公开数据整理,仅作展示用途。请用户自行辨别
✉️ 若企业需抹除展台内容或有异议, 请通过页面底部联系方式告知我们,我们会尽快处理。
第 1 / 1 页
现货

供应商参考报价(招募中)

品牌试剂参考报价(招募中)

📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

[参考文献]: A Sentissi, Et Al. Pentafluorobenzenesulfonyl Chloride: A New Electrophoric Derivatizing Reagent With Application To Tyrosyl Peptide Determination By Gas Chromatography With Electron Capture Detection. Anal Chem. 1984 Nov;56(13):2512-7.
[参考文献]: G B Baker, Et Al. Electron-Capture Gas Chromatographic Analysis Of Beta-Phenylethylamine In Tissues And Body Fluids Using Pentafluorobenzenesulfonyl Chloride For Derivatization. J Chromatogr. 1986 Sep 5;381(2):211-7.
[参考文献]: Kay Rittenbach, Et Al. A Rapid, Sensitive Electron-Capture Gas Chromatographic Procedure For Analysis Of Metabolites Of N-Methyl,N-Propargylphenylethylamine, A Potential Neuroprotective Agent. J Pharmacol Toxicol Methods. 2005 Nov-Dec;52(3):373-8.
[参考文献]: S J Asghar, Et Al. A Rapid Method Of Determining Amphetamine In Plasma Samples Using Pentafluorobenzenesulfonyl Chloride And Electron-Capture Gas Chromatography. J Pharmacol Toxicol Methods. 2001 Sep-Oct;46(2):111-5.
[参考文献]: Zhao-Qian Liu, Et Al. Simultaneous Determination Of Fluoxetine And Its Metabolite P-Trifluoromethylphenol In Human Liver Microsomes Using A Gas Chromatographic-Electron-Capture Detection Procedure. J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Apr 5;769(2):305-11.

合成参考文献


摘要:Kwiatkowska, M.; Kiełbasiński, P., Science of Synthesis: Knowledge Updates, (2024) 3, 436.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知