CAS: 156311-85-2; ((3H-[1,2,3]Triazolo[4,5-B]Pyridin-3-yl)Oxy)Tris(Dimethylamino)Phosphonium Hexafluorophosphate(V)

该化合物是一种化学化合物,其独特结构包括磷化和六氟磷酸阴离子;该化合物经常被用作有机合成的混合试剂,特别是在peptide合成和需要激活碳化物的其他应用中;其特性包括极地有机溶剂中的高溶性,这有利于其在各种化学反应中的使用; 氨三聚苯胺的出现有助于其稳定性和再活动,使其有效地促进核分裂性攻击; 此外,二甲基氨基化合物组加强了其核分离性,进一步协助其发挥联结剂的作用; 应当考虑安全因素,因为磷盐的潜在毒性和处理可能具有危险性的六氟磷酸.总的来说,合成有机化学对其促进复杂反应的效率和效果具有价值.

结构式图片

相似化合物

148893-10-1 873798-09-5 39968-33-7

欧盟法规

C&L通报

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:US-2019177392-A1
    优先权日:2014-09-23
    标 题 :Synthesis of glp-1 peptides
    发明人:PENIAS NAVON SHARON; NAVEH SHIRLY; VASILEIOU ZOI; BARLOS KONSTANTINOS
    权利人:NOVETIDE LTD
    摘要:Disclosed are processes for the synthesis of GLP-1 peptides, such as liraglutide and semaglutide, and a process for purifying liraglutide.

    专利号:US-2022233673-A1
    优先权日:2019-06-04
    标 题:METHODS OF PRODUCING SHIGA TOXIN B-SUBUNIT (STxB) MONOMERS AND OLIGOMERS, AND USES THEREOF
    发明人:BILLET ANNE; SCHMIDT FRÉDÉRIC; JOHANNES LUDGER; SERVENT DENIS; MOURIER GILLES; TARTOUR ÉRIC; KAY MICHAEL; FULCHER JAMES M
    权利人:INST CURIE; CENTRE NAT RECH SCIENT; INST NAT SANTE RECH MED; COMMISSARIAT A LENERGIE ATOMIQUE ET AUX ENERGIES ALTERNATIVES CEA; APHP ASSIST PUBLIQUE HOPITAUX DE PARIS; UNIV PARIS; UNIV OF UTAH RESEARCH FOUDATION; UNIV UTAH RES FOUND
    摘要:A method of producing a monomer of a Shiga toxin B-subunit (STxB) protein or of a variant thereof by peptide chemical synthesis, as well as to a method of producing a pentamer of the STxB protein or of the variant thereof. The methods are particularly advantageous as they overcome major issues typically observed in peptide chemical synthesis, including solubility and purity issues.

    专利号:US-10308595-B2
    优先权日:2013-02-15
    标 题:Albicidin derivatives, their use and synthesis
    发明人:SUESSMUTH RODERICH; KRETZ JULIAN; SCHUBERT VIVIEN; PESIC ALEXANDER; HUEGELLAND MANUELA; ROYER MONIQUE; COCIANCICH STEPHANE; ROTT PHILIPPE; KERWAT DENNIS; GRAETZ STEFAN
    权利人:UNIV BERLIN TECH
    摘要:Antibiotically active compounds characterized by general formula (I), wherein X1, BB, BC, BD, BE and X2 are building blocks with D1, D2, D3, D4 or D5 being linkers which include carbon, sulphur, nitrogen, phosphor and/or oxygen atoms and which are covalently connecting the moities BA and BB, BB and BC, BC and BD, BD and BE and BE and BF, respectively, and wherein in particular the building block BC comprises an amino acid derivative. The compounds for use in a method of treatment of diseases, in particular for use in a method of treatment of bacterial infections are also disclosed.

    专利号:US-2018057558-A1
    优先权日:2014-09-23
    标题 :Synthesis of GLP-1 Peptides
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    合成参考文献


    摘要:Lubell, W. D.; Blankenship, J. W.; Fridkin, G.; Kaul, R., Science of Synthesis, (2005) 21, 757.
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