CAS: 63995-70-0; Triphenylphosphine-3,3,3-Trisulfonic Acid Trisodium Salt Hydrate

该化合物是一种水溶磷衍生物,广泛用作悬浮和过渡金属催化,特别是在水相反应中.其全氟辛烷磺酸组会提高极地溶剂溶性,促进同质催化工艺.该化合物因其稳定性和与,金和等金属形成复合体的能力而备受重视,使其在交叉交错,氢化和水成形反应中有用. ~85%纯度确保合成应用的一贯性,同时保持成本效益. 它与环境友好反应介质的兼容性符合绿色化学原则. 妥善处理因其杂交性质而值得注意.

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

tris(natrium-m-sulfonatophenyl)phosphanoxid tris (3-ethyl phenyl sulfonate) phosphine triphenylphosphine 18H12Cl3O6PS3C18H12Cl3O6PS3(E)-3-phenylpropenal tris(natrium-m-sulfonatophenyl)phosphanoxid cinnamaldehydetrans-α,β-2H2cinnamaldehyde 16H14(2)HO9PS2(2-)*2Na(1+)C16H14(2)HO9PS2(2-)*2Na(1+)

合成工艺路线路线简述

  • 合成目标产物 Triphenylphosphine-3,3',3''-Trisulfonic Acid Trisodium Salt 主要起始原料 Triphenylphosphine
  • (文献来源)合成步骤主要原料 Triphenylphosphine
三苯基膦 反应生成 Sodium 3,3',3''-Phosphinetriyltribenzenesulfonate
参考文献:Bexten,L.;Cornils,B.;Kupies,D.
标题:Bexten,L.;Cornils,B.;Kupies,D.

海关参考信息

专利信息


专利号:US-5827794-A
优先权日:1994-02-22
标 题 :Supported highly-polar liquid phase chiral sulfonated binap catalyst for asymmetric synthesis of optically active compounds
发明人:DAVIS MARK E; WAN KAM TO
权利人:CALIFORNIA INST OF TECHN
摘要:The present invention relates to water soluble chiral sulfonated 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl and its use as organometallic catalysts for asymmetric synthesis of optically active compounds. Asymmetric reactions of the present invention include those reactions in which organometallic catalysts are commonly used. Such reactions include, but are not limited to, reduction and isomerization reactions on unsaturated substrates and carbon--carbon bond forming reactions. Examples of such reactions include, but are not limited to, hydrogenation, hydroboration, hydrosilylation, hydride reduction, hydroformylation, alkylation, allylic alkylation, arylation, alkenylation, epoxidation, hydrocyanation, disilylation, cyclization and isomerization reactions. n The catalysts of the present invention provide the advantage of functioning in the presence of water without loss in enantioselectivity relative to the nonsulfonated BINAP catalyst in an organic solvent. As a result, the catalysts of the present invention may be employed in water, water miscible solvents, in aqueous--organic two phase solvent systems and in supported aqueous phase catalysts in organic solvents without loss in enantioselectivity. Further, the catalysts of the present invention may also be effectively employed in highly polar solvents such as primary alcohols and ethylene glycol. n The present invention also relates to a method for conducting asymmetric reactions on prochiral unsaturated bonds contained within a compound using the water soluble chiral sulfonated 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl organometallic catalysts of the present invention.

专利号:US-7015321-B2
优先权日:2002-10-12
标 题 :Synthesis of non-symmetrical sulfamides using burgess-type reagents
发明人:NICOLAOU KYRIACOS C; LONGBOTTOM DEBORAH; SNYDER SCOTT A; HUANG XIANHAI
权利人:SCRIPPS RESEARCH INST
摘要:A practical and high-yielding method for the efficient, one-step synthesis of diverse classes of N,N′-differentiated sulfamides employs a wide range of amino alcohols and simple amines using Burgess-type reagents. This methodology extends the application and availability of sulfamides within the fields of chemical biology, medicinal chemistry, asymmetric synthesis, and supramolecular chemistry.

专利号:US-9346851-B2
优先权日:2008-02-22
标 题 :Chemical modification of proteins
发明人:BERNARDES GONCALO; CHALKER JUSTIN; DAVIS BENJAMIN
权利人:BERNARDES GONCALO; CHALKER JUSTIN; DAVIS BENJAMIN; RP SCHERER TECHNOLOGIES LLC
摘要:The invention relates to methods for selectively converting a cysteine residue in a peptide or protein to the dehydroalanine (Dha) residue. The method also works on selenocysteine and substituted cysteine and selenocysteine residues, resulting in the Dha residue which may be converted to any natural or unnatural amino acid residue desired without the alteration of the remainder of the peptide or protein. The invention also allows ligation of a desired peptide at any point rather than at a point where there should be a naturally occurring cysteine, thereby allowing native chemical ligation to be used in the synthesis of peptides that do not contain cysteine. The methodology allows for the synthesis of very large peptides.

专利号:US-11078178-B2
优先权日:2017-09-04
标 题 :6-chromanol derivatives and their synthesis
发明人:BEUMER RAPHAEL; BONRATH WERNER; DELPHO JAN-MARC; JORAY MARCEL; MEDLOCK JONATHAN ALAN; NETSCHER THOMAS; SORIANO DOMENICO; STEMMLER RENÉ TOBIAS
权利人:DSM IP ASSETS BV
摘要:The present invention relates to novel compounds which are particularly useful for the synthesis of novel chromanol derivatives. These compounds have interesting properties. Particularly, the novel chromanol derivatives have interesting antioxidant properties as well as flavours and fragrances.

专利号:EP-1314727-B1
优先权日:2001-11-23
标题 :Direct synthesis of quaternary phenanthridinium salts
发明人:CAPELLE NICOLAS; GALLO ROGER
权利人:MERIAL SAS
摘要:Process for the preparation of phenanthridinium quaternary salts (I) comprises reacting a halo-aromatic compound (II) with a phenyl boronic derivative (III) in a basic medium, in the presence of a palladium catalyst. Process for the preparation of phenanthridinium quaternary salts of formula (I) comprises reacting a halo-aromatic compound of formula (II) with a phenyl boronic derivative of formula (III) in a basic medium, in the presence of a palladium catalyst. R<3>, R<8> = an electro-attractor group having an electronegativity at last equal to that of nitro; R<5> = a non-chemically labile group; R<6> = aryl or 5-12C heteroaryl, which my be condensed and may have one or more hetero atoms; X<-> = a halide or hydrogen sulfate anion or a base joined to a mineral acid; X = halogen; R = H; R+R = a group of formula (i); n, n' = 0-4; R<9>, R<10> = H or 1-5C alkyl. Independent claims are also included for: (1) intermediates of formula (VI); and (2) the preparation of (VI). X1 = halogen.

专利号:US-4460786-A
优先权日:1980-07-10
标题 :Process for the selective addition of a compound having an activated carbon atom onto a substituted conjugated diene
发明人:MOREL DIDIER
权利人:RHONE POULENC IND
摘要:The selective addition of a compound having an activated carbon atom onto the carbon atom in the 4-position of a buta-1,3-diene carrying a hydrocarbon substituent on the carbon atom in the 2-position is achieved by reacting the compound having the activated carbon atom with the buta-1,3-diene carrying the hydrocarbon substituent in water or in an aqueous-alcoholic mixture in the presence of a catalyst which consists of at least one water-soluble phosphine and at least one rhodium compound, the catalyst being in solution in the water or aqueous alcoholic mixture. The products obtained are useful as precursors of intermediates for the synthesis of vitamins and perfumes.
邹平铭远进出口贸易有限公司
⚠️ 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.zoutong.com.cn
企业联系电话:0543-2240076👤
📞邹平铭远进出口贸易有限公司 ⚠️参考联系方式
联系人:徐立
电话:0543-2240076
手机:18763049273
传真:0543-2240079
邮箱:charliejqs@163.com
通信地址: 山东省邹平县城黛溪三路428号
邮编: 256200
🆔 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:山东省邹平县城黛溪三路428号
⚠️ 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:Negishi, E.; Wang, G., Science of Synthesis, (2009) 46, 332.
摘要:Palframan, M. J.; Parsons, A. F., Science of Synthesis, (2009) 48, 673.
摘要:Liang, Y.; Wen, Z.; Cabrera, M.; Howlader, A. H.; Wnuk, S. F., Science of Synthesis Knowledge Updates, (2020) 1, 330.
摘要:Liang, Y.; Wen, Z.; Cabrera, M.; Howlader, A. H.; Wnuk, S. F., Science of Synthesis Knowledge Updates, (2020) 1, 356.
摘要:Margaretha, P., Science of Synthesis Knowledge Updates, (2010) 4, 407.
📝 需求与反馈
尽可能描述清楚需求与问题信息
×

通知