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	<title>酞嗪 - 版本历史</title>
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	<updated>2026-04-20T17:34:51Z</updated>
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		<title>123.130.221.191：建立内容为“{{chembox | verifiedrevid = 408212873 |Reference=&lt;ref&gt;''Merck Index'', 11th Edition, '''7344'''.&lt;/ref&gt; |ImageFile=Phthalazin - Phthalazine.svg |ImageSize=180p…”的新页面</title>
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		<updated>2021-07-21T19:24:51Z</updated>

		<summary type="html">&lt;p&gt;建立内容为“{{chembox | verifiedrevid = 408212873 |Reference=&amp;lt;ref&amp;gt;&amp;#039;&amp;#039;&lt;a href=&quot;/index.php?title=Merck_Index&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;Merck Index（页面不存在）&quot;&gt;Merck Index&lt;/a&gt;&amp;#039;&amp;#039;, 11th Edition, &amp;#039;&amp;#039;&amp;#039;7344&amp;#039;&amp;#039;&amp;#039;.&amp;lt;/ref&amp;gt; |ImageFile=Phthalazin - Phthalazine.svg |ImageSize=180p…”的新页面&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新页面&lt;/b&gt;&lt;/p&gt;&lt;div&gt;{{chembox&lt;br /&gt;
| verifiedrevid = 408212873&lt;br /&gt;
|Reference=&amp;lt;ref&amp;gt;''[[Merck Index]]'', 11th Edition, '''7344'''.&amp;lt;/ref&amp;gt;&lt;br /&gt;
|ImageFile=Phthalazin - Phthalazine.svg&lt;br /&gt;
|ImageSize=180px&lt;br /&gt;
|IUPACName=Phthalazine&lt;br /&gt;
|OtherNames=Benzo-orthodiazine&amp;lt;br&amp;gt;2,3-Benzodiazine&amp;lt;br&amp;gt;Benzo[''d'']pyridazine&lt;br /&gt;
|Section1={{Chembox Identifiers&lt;br /&gt;
|  CASNo=253-52-1&lt;br /&gt;
|  PubChem=9207&lt;br /&gt;
|  SMILES=C1=CC=C2C=NN=CC2=C1&lt;br /&gt;
  }}&lt;br /&gt;
|Section2={{Chembox Properties&lt;br /&gt;
|  C=8|H=6|N=2&lt;br /&gt;
|  Appearance=浅黄色针状晶体&lt;br /&gt;
|  Density=&lt;br /&gt;
|  MeltingPtCL=90&lt;br /&gt;
|  MeltingPtCH=91&lt;br /&gt;
|  BoilingPtCL=315&lt;br /&gt;
|  BoilingPtCH=317&lt;br /&gt;
|  Boiling_notes=分解&lt;br /&gt;
|  Solubility=易溶于水&amp;lt;ref name=&amp;quot;Alfa&amp;quot;&amp;gt;{{Alfa|A12270|Datum=12. Juni 2013|Name=Phthalazine, 98%}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
|  pKa=3.39&amp;lt;ref&amp;gt;Brown, H.C., et al., in Baude, E.A. and Nachod, F.C., ''Determination of Organic Structures by Physical Methods'', Academic Press, New York, 1955.&amp;lt;/ref&amp;gt;&lt;br /&gt;
  }}&lt;br /&gt;
|Section3={{Chembox Hazards&lt;br /&gt;
|  MainHazards=&lt;br /&gt;
|  FlashPt=&lt;br /&gt;
|  Autoignition=&lt;br /&gt;
  }}&lt;br /&gt;
}}&lt;br /&gt;
'''酞嗪'''（'''Phthalazine'''）是一种[[杂环化合物]]，化学式C&amp;lt;sub&amp;gt;8&amp;lt;/sub&amp;gt;H&amp;lt;sub&amp;gt;6&amp;lt;/sub&amp;gt;N&amp;lt;sub&amp;gt;2&amp;lt;/sub&amp;gt;，由一个苯环与一个哒嗪环稠合而成。喹唑啉也可看做萘环的两个CH被N[[原子]]替换，这样的结构称为萘啶。酞嗪及其[[衍生物]]不存在于自然界。&amp;lt;ref name=&amp;quot;Raymond N. Castle&amp;quot;&amp;gt; {{cite | author = Raymond N. Castle | title = The Chemistry of Heterocyclic Compounds, Condensed Pyridazines Including ... | Publisher = John Wiley &amp;amp;amp; Sons | ISBN 047018848-0 = | year = 2009 | Online = {{Google Book | BuchID lQx33bsWwdMC = | page = 324}} | pages = 324ff}} &amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==合成==&lt;br /&gt;
&lt;br /&gt;
1,2-二(二溴甲基)苯与肼缩合，或用磷和氢碘酸还原氯酞嗪合成。&lt;br /&gt;
&lt;br /&gt;
==应用==&lt;br /&gt;
&lt;br /&gt;
酞嗪被用作有机合成的起始原料。&amp;lt;ref name=&amp;quot;Desmond J. Brown, Jonathan A. Ellman, Edward C. Taylor&amp;quot;&amp;gt; {{cite journal | author = Desmond J. Brown, Jonathan A. Ellman, Edward C. Taylor | title = Cinnolines and Phthalazines: Chemistry of Heterocyclic Compounds, Supplement II | publisher = John Wiley &amp;amp;amp; Sons | ISBN 047174411-5 = | year = 2005 | page = 175}}&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
==参考资料==&lt;br /&gt;
&lt;br /&gt;
{{reflist}}&lt;br /&gt;
{{环状化合物}}&lt;br /&gt;
[[Category:酞嗪| ]]&lt;br /&gt;
==参考来源==&lt;br /&gt;
*[http://zh.wikipedia.org/wiki/%E9%85%9E%E5%97%AA 维基百科-酞嗪]&lt;/div&gt;</summary>
		<author><name>123.130.221.191</name></author>
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