CAS: 3326-35-0; 3',6'-Dihydroxy-5-Nitro-3H-Spiro[isobenzofuran-1,9'-Xanthen]-3-One

该化合物是一个合成有机化合物,其特征是复杂的分子结构,包括异丙诺呋喃与Xantheon mothy之间的螺旋联系.该化合物具有两个氢氧基组和一个硝基组,有助于其化学反应和在各个领域的潜在应用.氢氧基组的存在通常会增加极地溶剂的溶性,并可能影响化合物的生物活动.硝基化合物可用作进一步的化学改变或反应的场所.该化合物因其独特的光学特性,经常被研究其在有机电子,染料或荧光探测器中的潜在用途.此外,其结构特性可能会产生有趣的光物理特性,从而引起材料科学和光化学学的兴趣.与许多有机化合物一样,由于潜在的毒性或回能性,应当观测安全和处理预防措施.

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上下游产品

CAS号610-27-5 4-硝基邻苯二甲酸 | CAS号108-46-3 间苯二酚 | CAS号5466-84-2 4-硝基邻苯二甲酸酐 | CAS号14926-29-5 5-硝基-二乙酸荧光素 | CAS号3326-34-9 5-氨基荧光素 | CAS号3326-32-7 异硫氰酸荧光素酯

合成工艺路线路线简述

    📜4-硝基邻苯二甲酸置于sodium Hydroxide体系中,用 甲醇 作为反应溶剂,化学反应 2.0H,反应生成 4-硝基荧光素
    参考文献:Fluorescent Human Ep3 Receptor Antagonists
    标题:Fluorescent Human Ep3 Receptor Antagonists
    摘要:Exchange Of The Lipophilc Part Of Ortho-Substituted Cinnamic Acid Lead Structures With Different Small Molecule Fluorophoric Moieties Via A Dimethylene Spacer Resulted In Hep(3)R Ligands With Affinities In The Nanomolar Concentration Range. Synthesized Compounds Emit Fluorescence In The Blue,Green,And Red Range Of Light And Have Been Tested Concerning Their Potential As A Pharmacological Tool. Hep(3)Rs Were Visualized By Confocal Laser Scanning Microscopy On Ht-29 Cells,On Murine Kidney Tissues,And On Human Brain Tissues And Functionally Were Characterized As Antagonists On Human Platelets. Inhibition Of Pge(2) And Collagen-Induced Platelet Aggregation Was Measured After Preincubation With Novel Hep(3)R Ligands. The Pyryllium-Labeled Ligand 8 Has Been Shown As One Of The Most Promising Structures,Displaying A Useful Fluorescence And Highly Affine Hep(3)R Antagonists.
    DOI:10.1021/ml300191G

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    专利信息


    专利号:WO-9509170-A1
    优先权日:1993-09-28
    标 题:Chemical synthesis of rhodamine derivatives
    发明人:CORRIE JOHN EDGAR THOMAS; CRAIK JAMES STANLEY
    权利人:MEDICAL RES COUNCIL; CORRIE JOHN EDGAR THOMAS; CRAIK JAMES STANLEY
    摘要:A method for preparing rhodamine derivatives of formulae (a) or (b) or a mixture of such compounds, where X is bromo, chloro- or iodoacetamido, maleimido, or amino. These compounds are the 5 and 6 (or 5' and 6') isomers of the amine, haloacetamide and maleimide derivatives of tetramethylrhodamine. The method enables for the first time the production of isomerically pure compounds on a relatively large scale. The products are fluorescent and are useful for the labelling of proteins.

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