CAS: 960-71-4; Triphenylborane

该化合物是有机有机体化合物,其特征是附于一个原子的三联苯组,似乎是白色的黄色固体,以其稳定性和水溶性低而著称,但在苯和甲苯等有机溶剂中可溶性较强.三联苯伯纳因其刘易酸特性而引人注目,允许其作为电子对接收器在各种化学反应中发挥作用.它通常用于有机合成,特别是用于形成含有钴的化合物,以及用作制备有机金属化合物的试剂.此外,它还用于光化学和某些聚合工艺中的催化剂,该化合物相对不有毒,但应谨慎处理,因为其可能造成皮肤和眼刺激.

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

diethyl ether dipropyl phenylboronate n-propylmagnesium bromide phenylborondichloride5,5,5-Triphenyl-1-pentanol Triphenyl-n-butylborate lithium salt 1,1,4,4-tetraphenyl-1,3-butadiene t-enyl)-boric acid ; tetramethylammonium salttriphenyl-(5,5,5-triphenyl-pent-2t-enyl)-boric acid ; tetramethylammonium salt

合成工艺路线路线简述

  • 合成目标产物 Triphenylborane 主要起始原料 Boron Trifluoride Diethyl Etherate And Phenylmagnesium Bromide
  • 33906-65-9 = 960-71-4
    反应条件:1.1 15 Min,200 °C
    标题:Stabilization And Transfer Of The Transient [mes*p4]- Butterfly Anion Using Bph3
    作者:Borger,Jaap E.; Ehlers,Andreas W.; Lutz,Martin; Slootweg,J. Chris; Lammertsma,Koop
    参考文献:Angewandte Chemie 日期:2016 卷标:55(2) 页码:613-617]

    = 960-71-4
    反应条件:1.1 Reagents: Triisopropyl Borate,Sodium Solvents: Toluene; 4 H,65 °C
    标题:Preparation Of Triphenylboron
    作者:Xu,Jiantao; Han,Minghan; Wang,Guogao
    参考文献:Shiyou Huagong 日期:2013 卷标:42(4) 页码:415-418]

    33906-65-9 = 960-71-4
    反应条件:1.1 -78 °C -> 200 °C; 15 Min,200 °C
    标题:Iron Complexes Of A Proton-Responsive Scs Pincer Ligand With A Sensitive Electronic Structure
    作者:Skubi,Kazimer L.; Hooper,Reagan X.; Mercado,Brandon Q.; Bollmeyer,Melissa M.; Macmillan,Samantha N.; Et Al
    参考文献:Inorganic Chemistry 日期:2022 卷标:61(3) 页码:1644-1658]

    87005-57-0 = 960-71-4 [标题:Reaction Conditions
    标题:Preparation Of Triarylboranes
    参考文献:United States]

    = 960-71-4
    反应条件:1.1 Reagents: Boron Trifluoride Etherate,Magnesium,Iodine Solvents: Xylene
    标题:Cost-Effective Preparation Method Of Triphenylboron Using Magnesium Powder And Bromobenzene
    参考文献:China]

    = 960-71-4
    反应条件:1.1 Reagents: Boron Trifluoride
    标题:Hydroxylamine-O-Sulfonic Acid
    作者:Erdik,Ender; Saczewski,Jaroslaw
    参考文献:E-Eros Encyclopedia Of Reagents For Organic Synthesis 日期:2013 卷标:1 页码:1-10]

    = 960-71-4
    反应条件:1.1 Reagents: Boron Trifluoride Etherate Solvents: Tetrahydrofuran; -20 °C
    标题:Photobase Generator
    参考文献:World Intellectual Property Organization]

    33906-65-9 = 960-71-4
    反应条件:1.1 Reagents: Mesitylene; 3 H,170 °C
    标题:Preparation Of Triarylboranes And Their Complexes By Thermal Decomposition Of Trialkylammonium Borates
    参考文献:Japan]

    971-66-4 = 960-71-4
    反应条件:1.1 Reagents: Mesitylene; 180 °C
    标题:Preparation Of Ionic-Impurity-Free Triarylborane Complexes
    参考文献:Japan]

    = 960-71-4
    反应条件:1.1 Reagents: Boron Trifluoride Etherate,Magnesium,Iodine Solvents: Diethyl Ether
    标题:Organoboranes. 44. A Convenient,Highly Efficient Synthesis Of Triorganylboranes Via A Modified Organometallic Route
    作者:Brown,Herbert C.; Racherla,Uday S.
    参考文献:Journal Of Organic Chemistry 日期:1986 卷标:51(4) 页码:427-32]

    = 960-71-4 [标题:Reaction Conditions
    标题:Boron Compounds. V. Hydrogenation Of Trialkyl- And Triarylboranes
    作者:Koester,Roland; Bruno,Guenter; Binger,Paul
    参考文献:Justus Liebigs Annalen Der Chemie 日期:1961 卷标:644 页码:1-22]

    = 960-71-4
    反应条件:1.1 Reagents: Triisopropyl Borate,Sodium Solvents: Benzene,Cyclohexane; Rt -> 80 °C; 40 Min,80 °C
    标题:Preparation Method Of Triarylborane
    参考文献:China]

    3262-89-3 = 960-71-4
    反应条件:1.1 Reagents: Potassium Carbonate Solvents: Dimethylformamide; 1 H,130 °C
    标题:Unexpected Formation Of Triphenylborane From Phenylboronic Acid And Its Use As An Intermediate In Palladium-Catalyzed Cross Coupling Reaction
    作者:Motokura,Ken; Fukuda,Takuma; Manaka,Yuichi
    参考文献:Chemistryselect 日期:2019 卷标:4(35) 页码:10501-10505]

    = 960-71-4
    反应条件:1.1 Reagents: Boron Trifluoride Solvents: Diethyl Ether; 0 °C; 2 H,0 °C; 0 °C -> Rt; Overnight,Rt
    标题:Controlling The Lewis Acidity And Polymerizing Effectively Prevent Frustrated Lewis Pairs From Deactivation In The Hydrogenation Of Terminal Alkynes
    作者:Liu,Qiang; Yang,Liu; Yao,Chenfei; Geng,Jiao; Wu,Youting; Et Al
    参考文献:Organic Letters 日期:2021 卷标:23(9) 页码:3685-3690]

    33906-65-9 = 960-71-4 [标题:Reaction Conditions
    标题:Crystal Structure Of Tetraphenyldiboroxane A Monomer Diboroxane
    作者:Lange,Thomas; Bohme,Uwe; Roewer,Gerhard
    参考文献:Inorganic Chemistry Communications 日期:2002 卷标:5(6) 页码:377-379]

    = 960-71-4 [标题:Reaction Conditions
    标题:Photosensitive Resin Composition With Excellent Curability
    参考文献:Japan]

    = 960-71-4 [标题:Reaction Conditions
    标题:Product Subclass 26: Aryl- And Hetarylboranes
    作者:Miyaura,N.
    参考文献:Science Of Synthesis 日期:2004 卷标:6 页码:677-696]

    = 960-71-4
    反应条件:1.1 Solvents: Chloroform-D
    标题:Borylated Carbodiimides
    作者:Einholz,Wolfgang; Haubold,Wolfgang
    参考文献:Zeitschrift Fuer Naturforschung 日期:1986 卷标:(11) 页码:1367-72]

    = 960-71-4
    反应条件:1.1 Reagents: Boron Trifluoride Etherate,Magnesium Solvents: Diethyl Ether
    标题:Ultrasonics In Organoborane Chemistry. Rapid Synthesis Of Triorganylboranes Via A Modified Organometallic Route
    作者:Brown,Herbert C.; Racherla,Uday S.
    参考文献:Tetrahedron Letters 日期:1985 卷标:26(36) 页码:4311-14]

    501-65-5 + 4151-77-3 = 960-71-4
    反应条件:1.1 Catalysts: Acetic Acid
    标题:Bora-Aromatic Systems. Vi. Dehalogenation Of Organoboron Dihalides In The Search For Borenes
    作者:Eisch,John J.; Becker,Hans P.
    参考文献:Journal Of Organometallic Chemistry 日期:1979 卷标:171(2) 页码:141-53
四苯硼钠置于hcl体系中,用 乙腈 作为反应溶剂,化学反应生成 三苯基硼烷
参考文献:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: Na: Svol.3,3.7,Page 1233-1245
标题:Gmelin Handbuch Der Anorganischen Chemie,Gmelin Handbook: Na: Svol.3,3.7,Page 1233-1245

海关参考信息

专利信息


专利号:US-11753503-B2
优先权日:2018-05-17
标 题:Supported onium salts as initiators for the synthesis of polycarbonates by copolymerization of CO2 with epoxides
发明人:FENG XIAOSHUANG; PATIL NAGANATHA; LUCIANI CAROLINE; GNANOU YVES; HADJICHRISTIDIS NIKOS
权利人:UNIV KING ABDULLAH SCI & TECH
摘要:Supported onium salts used as initiators for the synthesis of polycarbonates by copolymerization of carbon dioxide with epoxides are described. Embodiments of the present disclosure describe initiators comprising an insoluble portion including an onium cation attached to an insoluble support; and an anion, wherein the anion is a counter-ion to the onium cation. Embodiments further describe methods of making polycarbonates using the initiator, methods of making initiators, and the like.

专利号:US-2004006137-A1
优先权日:2002-06-28
标题:Asymmetric synthesis of amino-pyrrolidinones and a crystalline, free-base amino-pyrrolidinone
发明人:WALTERMIRE ROBERT E; CAMPAGNA SILVIO; SAVAGE SCOTT A; BORDAWEKAR SHAILENDRA; MADUSKUIE THOMAS P; DESIKAN SRIDHAR; ANDERSON STEPHEN R
摘要:A novel process for the asymmetric synthesis of an amino-pyrrolidinone of the type shown below is described. n n n These compounds are useful as intermediates for MMP and TACE inhibitors. n Crystalline, free-base form of Compound J ((2R)-2-((3R)-3-amino-3-{-[(2-methyl-4-quinolinyl)methoxy]phenyl}-2-oxopyrrolidinyl)-N-hydroxy-4-methylpentanamide): n n n which is useful as a TACE inhibitor, pharmaceutical compositions comprising the same, and methods of using the same for treating inflammatory diseases are also described.

专利号:US-11713329-B2
优先权日:2018-12-10
标 题 :Intermediates useful in the preparation of halichondrin compounds and methods for preparing the same
发明人:XU WEIPING
权利人:BEIJING TIENYI LUFU PHARMATECH CO LTD
摘要:The invention relates to intermediates useful in the preparation of halichondrin compounds, methods for preparing the same and use thereof, such as halichondrins, eribulin, or their analogs. The intermediates, the methods and use thereof are used for the synthesis of the C20-C26 fragment of halichondrin compounds. The raw materials in the synthetic route of the invention are cheap and easily obtained, the sources and the qualities of the raw materials are reliable. The choice of the methods useful in the synthesis of chiral central structures are based on the structural characteristics of the reactants, thus effectively improving the synthesis efficiency, reducing the difficulties and risks of product quality control, and avoiding the use of highly toxic and expensive organotin catalysts to significantly decrease costs and improve environmental friendliness.

专利号:US-7271231-B2
优先权日:1995-01-24
标 题 :Polymerization of olefins
发明人:BROOKHART MAURICE S; JOHNSON LYNDA KAYE; KILLIAN CHRISTOPHER MOORE
权利人:DU PONT
摘要:Disclosed herein are processes for polymerizing ethylene, acyclic olefins, and/or selected cyclic olefins, and optionally selected olefinic esters or carboxylic acids, and other monomers. The polymerizations are catalyzed by selected transition metal compounds, and sometimes other co-catalysts. Since some of the polymerizations exhibit some characteristics of living polymerizations, block copolymers can be readily made. Many of the polymers produced are often novel, particularly in regard to their microstructure, which gives some of them unusual properties. Numerous novel catalysts are disclosed, as well as some novel processes for making them. The polymers made are useful as elastomers, molding resins, in adhesives, etc. Also described herein is the synthesis of linear α-olefins by the oligomerization of ethylene using as a catalyst system a combination a nickel compound having a selected α-diimine ligand and a selected Lewis or Bronsted acid, or by contacting selected α-diimine nickel complexes with ethylene.

专利号:US-8697902-B2
优先权日:2008-06-17
标 题:Preparation of nitriles from ethylenically unsaturated compounds
发明人:MASTROIANNI SERGIO
权利人:MASTROIANNI SERGIO; RHODIA OPERATIONS
摘要:A process for the hydrocyanation of a hydrocarbon-based compound having at least one site of ethylenic unsaturation into a nitrile compound includes reaction thereof, in a liquid medium, with hydrogen cyanide in the presence of a catalyst containing a metal element selected from among the transition metals and an organophosphorus ligand, wherein the organophosphorus ligand is a compound of formula (I): n n n n n n n n n n The subject process is particularly useful for the synthesis of adiponitrile from butadiene.

专利号:US-8716507-B2
优先权日:2008-10-31
标题 :Iron(II) catalysts containing diimino-diphosphine tetradentate ligands and their synthesis
发明人:MIKHAILINE ALEXANDRE; FREUTEL FRIEDERIKE; SUI-SENG CHRISTINE; MEYER NILS; MORRIS ROBERT H; LAGADITIS PARASKEVI OLYMPIA
权利人:MIKHAILINE ALEXANDRE; FREUTEL FRIEDERIKE; SUI-SENG CHRISTINE; MEYER NILS; MORRIS ROBERT H; LAGADITIS PARASKEVI OLYMPIA; GOVERNING COUNCIL OF UNIVERSITY OF TORONTO
摘要:New hexa-coordinate iron (II) complexes comprising compounds of formula (I) are described. These compounds comprise a tetradentate ligand with donor atoms comprising nitrogen and phosphorus. These complexes are shown for the first time to be useful catalysts for the hydrogenation of ketones, aldehydes, or imines to produce alcohols or amines, and the asymmetric hydrogenation of prochiral ketones or imines to produce non-racemic alcohols or amines. The source of the hydrogen can be hydrogen gas or a hydrogen-donating molecule such as isopropanol or hydrogen-donating mixture such as formic acid and an amine depending on the structure of the catalyst. In certain embodiments, the axial ligands on the catalyst comprise organonitrile ligands, carbonyl ligands, isonitrile ligands, or combinations thereof. The catalysts and the preparation thereof are disclosed. A reaction using phosphine and diamine precursors that is templated by the iron ion is the preferred route to the catalysts.
郑州今斯孚化学有限公司
⚠️ 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.kingsfine.com/index.html
电话: 0371-56632527 13838252817👤
📞郑州今斯孚化学有限公司 ⚠️参考联系方式

销售电话:0371-56632527 13838252817
邮箱:sales@kingsfine.com
🆔 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→

⚠️ 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。
北京国方鼎盛科技有限公司
⚠️ 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.gfdschem.com
企业联系电话:18610472091👤
📞北京国方鼎盛科技有限公司 ⚠️参考联系方式
联系人:方经理
电话:18610472091
手机:18610472091
传真:010-59092859
邮箱:gfdschem@126.com
通信地址: 北京市中关村科技园大兴区生物医药基地天荣街19号1号楼
邮编: 100026
🆔 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:北京市中关村科技园大兴区生物医药基地天荣街19号1号楼
⚠️ 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

合成参考文献


摘要:Stolley, R. M.; Louie, J., Science of Synthesis Knowledge Updates, (2013) 2, 39.
摘要:Ramirez y Medina, I.-M.; Kipke, W.; Makow, J.; Staubitz, A., Science of Synthesis Knowledge Updates, (2020) 2, 33.
摘要:Ulfkjær, A.; Pittelkow, M., Science of Synthesis Knowledge Updates, (2018) 1, 134.
摘要:Tauchert, M. E., Science of Synthesis: C-1 Building Blocks in Organic Synthesis, (2013) 1, 313.
摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知