![]() 5-溴-2-硝基吡啶结构式
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常用名 | 5-溴-2-硝基吡啶 | 英文名 | 5-Bromo-2-nitropyridine |
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CAS号 | 39856-50-3 | 分子量 | 202.99 | |
密度 | 1.8±0.1 g/cm3 | 沸点 | 292.3±20.0 °C at 760 mmHg | |
分子式 | C5H3BrN2O2 | 熔点 | 148-150 °C(lit.) | |
MSDS | 中文版 美版 | 闪点 | 130.6±21.8 °C | |
符号 |
![]() GHS07 |
信号词 | Warning |
A simple Cu-catalyzed coupling approach to substituted 3-pyridinol and 5-pyrimidinol antioxidants.
J. Org. Chem. 73(23) , 9326-33, (2008) A convenient approach to 3-pyridinols and 5-pyrimidinols via a two-step Cu-catalyzed benzyloxylation/catalytic hydrogenation sequence is presented. The corresponding 3-pyridinamines and 5-pyrimidinamines can be prepared in an analogous sequence utilizing benz... |
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Structure-activity relationship study of EphB3 receptor tyrosine kinase inhibitors.
Bioorg. Med. Chem. Lett. 19 , 6122, (2009) A structure-activity relationship study for a 2-chloroanilide derivative of pyrazolo[1,5-a]pyridine revealed that increased EphB3 kinase inhibitory activity could be accomplished by retaining the 2-chloroanilide and introducing a phenyl or small electron dona... |
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FT-Raman and FT-IR spectra, vibrational assignments and density functional studies of 5-bromo-2-nitropyridine. Sundaraganesan N, et al.
Spectrochim. Acta A 61(13) , 2995-3001, (2005)
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Synthesis of fluorine-18-labelled 5-and 6-fluoro-2-pyridinamine. Abrahim A, et al.
J. Labelled Comp. Radiopharm. 49(4) , 345-356, (2006)
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Structure-based design and synthesis of the first weak non-phosphate inhibitors for IspF, an enzyme in the non-mevalonate pathway of isoprenoid biosynthesis. Baumgartner C, et al.
Helv. Chim. Acta 90(6) , 1043-1068, (2007)
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