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  4. 2-Amino benzamidoxime

2-Amino benzamidoxime  (Synonyms: ABAO)

目录号: HY-125372
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2-Amino benzamidoxime (ABAO compound 6) 能够与醛类快速反应，在水溶液中形成稳定的 1,2-二氢喹唑啉-3-氧化物 (dihydroquinazoline derivative)。2-Amino benzamidoxime 反应过程包括形成席夫碱 (Schiff base) 作为速率决定步骤，随后是快速的分子内环化。反应速率与 pH 值有关，表明质子化的苯酰胺肟 (protonated benzamidoxime) 作为内部广义酸参与席夫碱的形成。芳香环上的取代基可以增加芳香胺的碱性，从而加速反应。2-Amino benzamidoxime 的反应特性使其有潜力作为一种平台，用于开发新的生物共轭策略、荧光探针以及遗传编码库的翻译后多样化。

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2-Amino benzamidoxime Chemical Structure

2-Amino benzamidoxime Chemical Structure

CAS No. : 16348-49-5

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2-Amino benzamidoxime 相关抗体

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  • 生物活性

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生物活性

2-Amino benzamidoxime (ABAO compound 6) can react quickly with aldehydes to form stable 1, 2-dihydroquinazoline 3-oxides in aqueous solutions. The 2-Amino benzamidoxime reaction process consists of the formation of a Schiff base as a rate-determining step, followed by rapid intramolecular cyclization. The reaction rate is dependent on pH, indicating that protonated benzamidoxime is involved in the formation of Schiff bases as an internal generalized acid. Substituents on the aromatic ring can increase the alkalinity of the aromatic amine, thus speeding up the reaction. The reactive properties of 2-Amino benzamidoxime make it a potential platform for the development of new bioconjugated strategies, fluorescent probes, and post-translational diversification of genetic coding libraries[1].

分子量

151.17

Formula

C7H9N3O
CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.
纯度 & 产品资料
参考文献

2-Amino benzamidoxime 相关分类

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Keywords:

2-Amino benzamidoxime16348-49-5ABAOBiochemical Assay ReagentsSchiff baseFluorescent probeprotein bioconjugationBioorthogonal chemistryInhibitorinhibitorinhibit

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