化学
试剂
酮
合成子
惰性气体
转鼓
有机化学
腙
环加成
溶解度
药物化学
催化作用
亲核细胞
作者
A. Richard Chamberlin,James E. Sheppeck,Brian C. Goess,Chulbom Lee
出处
期刊:
日期:2007-09-14
被引量:2
标识
DOI:10.1002/047084289x.rt137.pub2
摘要
[1576-35-8] C7H10N2O2S (MW 186.26) InChI = 1S/C7H10N2O2S/c1-6-2-4-7(5-3-6)12(10,11)9-8/h2-5,9H,8H2,1H3 InChIKey = ICGLPKIVTVWCFT-UHFFFAOYSA-N (used as a source of diazene;2 condensed with ketones and aldehydes to form hydrazones that can be converted into reactive intermediates such as diazoalkanes, carbenes, carbenium ions, alkyllithiums, or umpolung synthons;7 used in 1,3-dipolar cycloaddition reactions to form N-heterocycles; used to make propargyl aldehydes and ketones via the Eschenmoser fragmentation;44 ketone hydrazones are deoxygenated with mild reagents in a modified Wolff–Kishner reduction50) Alternate Name: tosyl hydrazide. Physical Data: mp 108–110 °C (dec). Solubility: sol virtually all organic solvents except hydrocarbons; insol water. Form Supplied in: solid; widely available. Handling, Storage, and Precautions: is thermally labile at elevated temperatures, but can be stored at or below room temperature. It is a toxic, potentially flammable solid which should be handled with gloves under inert atmosphere.
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