CAS: 139332-66-4; 4-Nitro-7-(Piperazin-1-yl)Benzo[c][1,2,5]Oxadiazole
该化合物是一种异环化合物,其核心为苯氧二氮醇,与硝基化合物和氟硝酸盐合金具有功能作用.这种结构具有独特的电子和结合特性,在有机合成和材料科学中具有价值.硝基苯组增强了进一步功能化的再活性,而管状子替代组则提高了溶性,并为衍生提供了多功能处理器.其荧光学特性在探测设计和感测应用中很有意义.该化合物的稳定性和定义明确的再活性特征使其适合用作制药,农用化学品和高级材料研究的建筑块.
- 英文名称4-Nitro-7-(Piperazin-1-yl)Benzo[c][1,2,5]Oxadiazole
- 中文名称4-硝基-7-哌嗪苯并氧杂噁二唑
- IUPAC名称4-nitro-7-(piperazin-1-yl)benzo[c][1,2,5]oxadiazole
- 其它别名4-Methyl-3-Phenyl-2-(Pyridin-3-yl)Pentanenitrile; 4-Nitro-7-(Piperazin-1-yl)-2,1,3-Benzoxadiazole; 4-Nitro-7-Piperazinobenzofurazan; 4-Nitro-7-Piperazin-1-Yl-2,1,3-Be
- CAS编号139332-66-4
- MFCD编号:MFCD00191507
- EINECS号:635-064-4
- 分子式:C10H11N5O3分子量:249.23
- 产品CID: 608900
- 产品分类分析化学 → 液相色谱 → HPLC标记试剂
物理性质
MSDS等安全信息
欧盟法规
ECHA物质C&L通报上下游产品
CAS号110-85-0 哌嗪 | CAS号10199-89-0 4-氯-7-硝基-2,1,3-... | CAS号142-64-3 哌嗪二盐酸盐单水合物 | CAS号871508-91-7 4-(7-nitrobenzo...合成工艺路线路线简述
📜4-(7-Nitrobenzo[1,2,5]Oxadiazol-4-yl)Piperazine-1-Carboxylic Acid Tert Butyl Ester置于三氟乙酸体系中,化学反应生成4-硝基-7-哌嗪苯并氧杂噁二唑
参考文献:A Highly Selective And Sensitive Fluorescent Probe For Simultaneously Distinguishing And Sequentially Detecting H2S And Various Thiol Species In Solution And In Live Cells
标题:A Highly Selective And Sensitive Fluorescent Probe For Simultaneously Distinguishing And Sequentially Detecting H2S And Various Thiol Species In Solution And In Live Cells
摘要:一种新型的双通道线粒体靶向荧光探针(ncr)被合理设计,可同时区分和顺序感知h2S,Cys/hcy和gsh.
Doi:10.1039/c8Cc07761D
海关参考信息
- 2921211000-乙二胺
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合成参考文献
参考文献:10.1074/jbc.m604372200
摘要:Turella P, Filomeni G, Dupuis ML, Ciriolo MR, Molinari A, De Maria F, Tombesi M, Cianfriglia M, Federici G, Ricci G, Caccuri AM. A strong glutathione S-transferase inhibitor overcomes the P-glycoprotein-mediated resistance in tumor cells. 6-(7-Nitro-2,1,3-benzoxadiazol-4-ylthio)hexanol (NBDHEX) triggers a caspase-dependent apoptosis in MDR1-expressing leukemia cells. J Biol Chem. 2006 Aug 18;281(33):23725–32. doi: 10.1074/jbc.m604372200.
参考文献:10.1155/2007/71943
摘要:Stockwell PB. Abstracts of Papers Presented at the 2007 Pittsburgh Conference. Journal of Automated Methods and Management in Chemistry. 2007;2007():1–85. doi: 10.1155/2007/71943.
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