(E)-N-(2-Fluoro-5-((3-(2-(pyri
din-2-yl)vinyl)-1H-indazol-6-yl)amino)phenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide- 询价
- 进口原装
- 欧美
- ZMX-132640
- 2025年07月14日
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- 英文名：
(E)-N-(2-Fluoro-5-((3-(2-(pyridin-2-yl)vinyl)-1H-indazol-6-yl)amino)phenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide
- 库存：
1
- 供应商：
上海甄准
- CAS号：
319460-94-1
- 规格：
5g
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文献和实验Synthesis of -Vinyl Amino Acids
This chapter presents procedures for the synthesis of α-vinyl amino acids, in which the usual α-proton is replaced by an unsubstituted vinyl group (Fig. 1 ). The parent member of this family, α-vinylglycine (R≠H), is a natural product
Precolumn derivatization of amino acids followed by their resolution by reverse-phase high-performance liquid chromatography (RP-HPLC) is now the preferred method for quantitative amino acid analysis. The derivatization step introduces
has been riddled with assay limitations. Here, we describe application of a 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium cell viability assay to study cytotoxicity of various carbon-based nanomaterials on cells
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