Also known as triazines
right|frame|class=skin-invert|The three isomers of triazine, with ring numbering Triazines are a class of nitrogen-containing heterocycles. The parent molecules' molecular formula is . They exist in three isomeric forms, 1,3,5-triazines being common.
Research
33,281 papers- s-Triazine: A Privileged Structure for Drug Discovery and Bioconjugation.Molecules (Basel, Switzerland) · 2021
- Advances in the Chemistry of 2,4,6-Tri(thiophen-2-yl)-1,3,5-triazine.ChemistryOpen · 2023
- Antitumor Activity of s-Triazine Derivatives: A Systematic Review.Molecules (Basel, Switzerland) · 2023
- Triazine as a promising scaffold for its versatile biological behavior.European journal of medicinal chemistry · 2015
- The Chemistry of Triazine Isomers: Structures, Reactions, Synthesis and Applications.Mini reviews in medicinal chemistry · 2020
via PubMed
Wikidata facts
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- topic's main category
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- Encyclopædia Britannica 11th edition
Sources (2)
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Article · 中文
三嗪(英語:Triazine)是含有三个氮原子的六元杂环化合物,分子式为C3H3N3,有三种异构体: * ,也称“连三嗪”; * ,也称“偏三嗪”、“不对称三嗪”; * 1,3,5-三嗪,也称“均三嗪”、“对称三嗪”。 1,2,3-及1,2,4-三嗪均未见其单独存在,但衍生物都已制得。1,2,3-三嗪可由2-叠氮基环丙烯类化合物热作用下的重排得到。1,2,4-三嗪可由α-二羰基化合物和氨基脲(或氨基胍)缩合得到,也可通过Bamberger三嗪合成制取。1,3,5-三嗪由三分子氢氰酸聚合生成,衍生物也一般由XCN三聚制取(X=H、卤素、R、Ar、NH2、OH等)。 三嗪环上不易进行亲电芳香取代反应,但易发生亲核芳香取代反应。均三嗪的光谱结果与苯很相像,环为平面结构,C-N键长相等,但键角NCN比CNC大。它对热稳定,但遇水迅速发生水解,生成甲酸和氨。因此,均三嗪的2,4,6-三氯取代物(三聚氰氯)是由氯化氰三分子聚合制取的。三聚氰氯是常用的化工原料,氯原子容易发生亲核取代反应,且三个氯的活性依次降低,可通过控制条件获得想要的产物。它用水蒸气水解得到三聚氰酸;碱性室温水解得到6-羟基-2,4-二氯均三嗪钠盐;100°C与氨作用生成三聚氰胺;与酚、醇、胺亦可缩合,生成的产物用作活性染料、塑料、除草剂、荧光增白剂、坚膜剂等。 1,2,4-三嗪类可与富电子的亲双烯体发生Diels-Alder反应,经由双环的中间体,放出氮气,得到另一个芳香化合物。以炔烃作原料,1,2,4-三嗪可转化为吡啶环。
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