CAS: 182482-25-3; 2,4,6-Trifluorophenylboronic Acid

该化合物是一种氟化丙烯酸衍生物,在铃木-宫浦交叉相交反应中广泛用作关键中间体.它的电子缺氧芳香环,由于存在三种氟替代成分,增强了酸催化变异的回活动,使其对建造复杂的氟化双aryl结构很有价值.该化合物在标准条件下表现出了良好的稳定性,在组合反应中具有很高的选择性.在制药和农用化学研究中,它特别有用,因为人们往往希望在代谢稳定性和生物活性方面使用氟芳烃运动模式.产品通常以白色到非白晶状的纯度高纯度供应,确保合成应用的可靠性能.

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CAS号2367-76-2 1-溴-2,4,6-三氟苯 | CAS号121-43-7 硼酸三甲酯 | CAS号372-38-3 1,3,5-三氟苯 | CAS号363-72-4 五氟苯 | CAS号1206164-33-1 2,4,6-trifluoro... | CAS号49602-47-3 1-methoxy-2-(4-...

合成工艺路线路线简述

    2,4,6-Trifluorophenyl Trifluoroborate 以 Phosphate Buffer 用作溶剂,化学反应生成2,4,6-三氟苯硼酸
    参考文献:Substituent Effects On Aryltrifluoroborate Solvolysis In Water: Implications For Suzuki−miyaura Coupling And The Design Of Stable 18F-Labeled Aryltrifluoroborates For Use In Pet Imaging
    标题:Substituent Effects On Aryltrifluoroborate Solvolysis In Water: Implications For Suzuki−miyaura Coupling And The Design Of Stable 18F-Labeled Aryltrifluoroborates For Use In Pet Imaging
    摘要:Whereas Electron Withdrawing Substituents Retard The Rate Of Aryltrifluoroborate Solvolysis,Electron-Donating Groups Enhance It. Herein Is Presented A Hammett Analysis Of The Solvolytic Lability Of Aryltrifluoroborates Where Log(K(Solv)) Values Correlate To Sigma Values With A Rho Value Of Approximately-1. This Work Provides A Predictable Rubric For Tuning The Reactivity Of Boron For Several Uses Including F-18-Labeled Pet Reagents And Has Mechanistic Implications For Arbf3-Enhanced Ligandless Metal-Mediated Cross Coupling Reactions With Aryltrifluoroborates.
    Doi:10.1021/jo800681D

    专利信息


    专利号:WO-2025006693-A1
    优先权日:2023-06-30
    标 题 :Cannabidiol-like compounds and methods for the selective preparation of the same
    发明人:CHITTIBOYINA AMAR G; CHATTERJEE SHAMBA; PANDEY PANKAJ; KHAN IKHLAS A
    权利人:UNIV MISSISSIPPI
    摘要:In one aspect, the disclosure relates to new cannabidiol (CBD) analogs produced from allylic monoterpene alcohols and substituted resorcinols in the presence of aryl boronic acids, efficient and mild synthetic methods of making the new CBD analogs, and improved methods of making known CBD analogs. In one aspect, the methods produce low amounts of tetrahydrocannabinol (THC)-like compounds, low amounts of abnormal cannabidiol (abn-CBD) analogs, and higher amounts of CBD analogs, greatly simplifying purification. The methods can be tailored further to produce low amounts of CBD analogs and higher amounts abn-CBD analogs. In the disclosed methods, synthesis parameters can be varied in order to selectively produce a desired normal or abnormal regioisomer.

    专利号:US-9856241-B2
    优先权日:2013-07-03
    标 题:Substituted benzofuranyl and benzoxazolyl compounds and uses thereof
    发明人:BALOGLU ERKAN; SHACHAM SHARON; SENAPEDIS WILLIAM; MCCAULEY DILARA; LANDESMAN YOSEF; GOLAN GALI; KALID ORI; SHECHTER SHARON
    权利人:KARYOPHARM THERAPEUTICS INC
    摘要:The invention generally relates to substituted benzofuranyl and substituted benzoxazolyl compounds, and more particularly to a compound represented by Structural Formula (A): or a pharmaceutically acceptable salt thereof, wherein the variables are as defined and described herein. The invention also includes the synthesis and use of a compound of Structural Formula (A), or a pharmaceutically acceptable salt or composition thereof, e.g., in the treatment of cancer (e.g., mantle cell lymphoma), and other diseases and disorders.
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    2,4,6-三氟苯硼酸
    2,4,6-Trifluorophenylboronic acid
    产品图片纯度:98
    250kg/drum
    第 1 / 1 页

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    合成参考文献


    参考文献:10.1021/cg501132d
    摘要:Madura ID, Czerwińska K, Sołdańska D. Hydrogen-Bonded Dimeric Synthon of Fluoro-Substituted Phenylboronic Acids versus Supramolecular Organization in Crystals. Crystal Growth & Design. 2014 Oct 21;14(11):5912–21. doi: 10.1021/cg501132d.
    参考文献:10.1007/s00706-025-03388-4
    摘要:Ostojic J, Herenda S, Gojak-Salimović S, Pržulj S, Galijasevic S, Miloš M. Exploring the inhibition potential of 2,4,6-trifluorophenylboronic acid on horseradish peroxidase. Monatsh Chem. 2025 Nov 06;156(12):1365–71. doi: 10.1007/s00706-025-03388-4.
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