CAS: 166172-69-6; Bis[3,5-Bis(Trifluoromethyl)Phenyl]Phosphane

该化合物是一个磷化合物,其独特的结构特征是,与中磷原子相连,有两组3,5-双(三氟甲基)苯基,其结构独特,结构为3,5-双(三氟甲基)苯基,与中磷原子相连,该化合物因其高电离子三氟甲基组而显著地影响其反应性和稳定性,这些组的存在增强了分子的亲和热稳定性,使之适合有机合成和催化的各种应用.此外,苯基组体的体积性质可造成阻塞,影响其与金属中心的协调性.作为磷的分解和分解,可参与化学协调,形成转化金属的复杂体,这些金属在催化和材料科学中具有价值.该化合物的处理通常受到与磷及其衍生物的潜在毒性有关的护理.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

bis(3,5-di(trifluoromethyl)phenyl)chlorophosphine bis[3,5-bis(trifluoromethyl) phenyl]phosphine oxide 3,6-bis(trifluoromethyl)bromobenzene 22H20F12NPC22H20F12NPphosphino>methyl>-1,1'-biphenyl2,2'-bisphosphinomethyl-1,1'-biphenyl Bis-(3,5-bis-trifluoromethyl-phenyl)-vinyl-phosphane P,P'-(1,2-ethanediyl)bis{bis[3,5-di(trifluoromethyl)phenyl]phosphane} 3-[bis-(3,5-bis-trifluoromethyl-phenyl)-phosphanyl]-propan-1-ol

合成工艺路线路线简述

    📜在 硼烷四氢呋喃络合物体系中,用 二氯甲烷 用作溶剂,化学反应 1.0H,反应生成双(3,5-二(三氟甲基)苯基)膦
    参考文献:桦木还原过程中二芳基次膦酸-硼烷酰胺的非对映选择性脱对称†
    标题:桦木还原过程中二芳基次膦酸-硼烷酰胺的非对映选择性脱对称†
    摘要:用碱金属溶液在液氨中处理具有手性酰胺基官能团的二芳基次膦酸-硼烷酰胺会诱导一个芳基取代基在磷上优先脱芳香化,导致形成非等摩尔量的非对映异构体.脱芳香化的非对映选择性很大程度上取决于手性助剂的结构.
    Doi:10.1039/c4Ob02440K

    海关参考信息

    专利信息


    专利号:US-12202782-B2
    优先权日:2020-11-19
    标 题:Processes and intermediates for preparing MCL1 inhibitors
    发明人:DIXON DARRYL D; ISCHAY MICHAEL A; JOHNSON TREVOR C; MERIT JEFFREY E; REGENS CHRISTOPHER S; STANDLEY ERIC A; STEINHUEBEL DIETRICH P
    权利人:GILEAD SCIENCES INC
    摘要:The present disclosure relates to methods and intermediates for the synthesis of certain compounds that inhibit MCL1, for use in the treatment of cancers.

    专利号:US-11780834-B2
    优先权日:2018-06-21
    标题:Solid forms of 3-((1R,3R)-1-(2,6-difluoro-4-((1-(3-fluoropropyl)azetidin-3- yl)amino)phenyl)-3-methyl-1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indol-2-yl)-2,2-difluoropropan-1-ol and processes for preparing fused tricyclic compounds comprising a substituted phenyl or pyridinyl moiety, including methods of their use
    发明人:CHUNG CHEOL KEUN; XU JIE; IDING HANS; CLAGG KYLE; DALZIEL MICHAEL; FETTES ALEC; GOSSELIN FRANCIS; LIM NGIAP-KIE; MCCLORY ANDREW; ZHANG HAIMING; CHAKRAVARTY PAROMA; NAGAPUDI KARTHIK; ROBINSON SARAH
    权利人:HOFFMANN LA ROCHE; GENENTECH INC
    摘要:Provided herein are solid forms, salts, and formulations of 3-((1R,3R)-1-(2,6-difluoro-4-((1-(3-fluoropropyl)azetidin-3-yl)amino)phenyl)-3-methyl-1,3,4,9-tetrahydro-2H-pyrido[3,4-b]indol-2-yl)-2,2-difluoropropan-1-ol, processes and synthesis thereof, and methods of their use in the treatment of cancer.

    专利号:US-9062085-B2
    优先权日:2010-09-10
    标 题 :Biaryl diphosphine ligands, intermediates of the same and their use in asymmetric catalysis
    发明人:ABDUR-RASHID KAMALUDDIN; JIA WENLI; LU SHUIMING; GUO RONGWEI; CHEN XUANHUA; AMOROSO DINO
    权利人:ABDUR-RASHID KAMALUDDIN; JIA WENLI; LU SHUIMING; GUO RONGWEI; CHEN XUANHUA; AMOROSO DINO; KANATA CHEMICAL TECHNOLOGIES INC
    摘要:The present disclosure relates to biaryl diphosphine ligands of the formula (B), processes for the production of the ligands and the use of the ligands in metal catalysts for asymmetric synthesis. The disclosure also relates to intermediates used for the production of the biaryl diphosphine ligand. (Formula (B))

    专利号:US-9962690-B2
    优先权日:2014-04-27
    标题:N-substituted pyridiniophosphines, processes for their preparation and their use
    发明人:ALCARAZO MANUEL; WILLE CHRISTIAN; TINNERMANN HENDRIK
    权利人:STUDIENGESELLSCHAFT KOHLE MBH
    摘要:The present invention deals with the synthesis and applications of new cationic compounds being useful as metal ligands. Specifically, N-alkyl/aryl substituted pyridiniophosphines are prepared and used as ligands for transition metals. The so-obtained metal complexes and their use as catalysts in chemical synthesis is also described. It also worth mentioning that N-alkyl/aryl pyridiniophosphines can be synthesized through a short, scalable and highly modular route.

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    📌 第三方产品分析报告

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    合成参考文献


    参考文献:10.1007/s11696-024-03369-7
    摘要:Muzammil, Zahoor AF, Parveen B, Javed S, Akhtar R, Tabassum S. Recent developments in the chemistry of Negishi coupling: a review. Chem. Pap. 2024 Mar 10;78(6):3399–430. doi: 10.1007/s11696-024-03369-7.
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