CAS: 528-71-2; 1-Hydroxyphenazine

该化合物是一种杂交循环化合物,在1号位置用一个氢氧基组替代苯丙胺核心,这种结构具有独特的红氧化特性和电子转移能力,在有机合成,染色化学和电化学研究等应用中具有价值,其结合系统可增强稳定性和反应性,特别是在催化和光化工艺中. Pheenazin-1-ol 也被用作具有定制电子或生物特性的衍生物合成的前体.该化合物的明确界定的分子结构和功能组多功能组有助于其在研究和工业环境中的效用,特别是在需要对红氧化行为或光学特性进行精确控制的情况下.

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合成工艺路线路线简述

    📜2-硝基苯甲醚置于氢氧化钾,氢溴酸,溶剂黄146,苯体系中,化学反应生成 1-羟基吩嗪
    参考文献:Yosioka,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1952,Vol. 72,P. 1128,1130
    标题:Yosioka,Yakugaku Zasshi/journal Of The Pharmaceutical Society Of Japan,1952,Vol. 72,P. 1128,1130

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    1. Ramafi, G., Anderson, R., Theron, A., et al. Exposure of N-formyl-L-methionyl-L-leucyl-L-phenylalanine-activated human neutrophils to the Pseudomonas aeruginosa-derived pigment 1-hydroxyphenazine is associated with impaired calcium efflux and potentiation of primary granule enzyme release. Infect. Immun. 67(10), 5157-5162 (1999). 2. Sinha, S., Shen, X., Gallazzi, F., et al. Generation of reactive oxygen species mediated by 1‑hydroxyphenazine, a virulence factor of Pseudomonas aeruginosa. Chem. Res. Toxicol. 28(2), 175-181 (2015). 3. Munro, N.C., Barker, A., Rutman, A., et al. Effect of pyocyanin and 1-hydroxyphenazine on in vivo tracheal mucus velocity. J. Appl. Physiol. 67(1), 316-323 (1985). 4. Luo, Q., Hu, H., Peng, H., et al. Isolation and structural identification of two bioactive phenazines from Streptomyces griseoluteus P510. Chin. J. Chem. Eng. 23(4), 699-703 (2015).

    合成参考文献


    参考文献:10.1155/2014/682946
    摘要:Dharni S, Sanchita, Samad A, Sharma A, Patra DD. The Interaction Pattern between a Homology Model of 40S Ribosomal S9 Protein ofRhizoctonia solaniand 1-Hydroxyphenaize by Docking Study. BioMed Research International. 2014;2014():1–6. doi: 10.1155/2014/682946.
    参考文献:10.1007/s00284-020-02162-5
    摘要:Gong D, Ye F, Pang C, Lu Z, Shang C. Isolation and Characterization of Pseudomonas sp. Cr13 and Its Application in Removal of Heavy Metal Chromium. Curr Microbiol. 2020 Nov;77(11):3661–70. doi: 10.1007/s00284-020-02162-5.
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