![]() 2-Bromo-3-nitropyridine structure
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Common Name | 2-Bromo-3-nitropyridine | ||
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CAS Number | 19755-53-4 | Molecular Weight | 202.993 | |
Density | 1.8±0.1 g/cm3 | Boiling Point | 244.0±20.0 °C at 760 mmHg | |
Molecular Formula | C5H3BrN2O2 | Melting Point | 122-125 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 101.4±21.8 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Furanylazaindoles: potent anticancer agents in vitro and in vivo.
J. Med. Chem. 56(20) , 8008-18, (2013) Preliminary biological data on 7-anilino-6-azaindoles (8-11) suggested that hydrophobic substituents at C7 contribute to enhancement of antiproliferative activity. A novel series of 7-aryl-6-azaindole-1-benzenesulfonamides (12-22) were developed and showed im... |
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Synthesis and biological evaluation of N-arylbenzo[b]thieno[3,2-d]pyrimidin-4-amines and their pyrido and pyrazino analogues as Ser/Thr kinase inhibitors.
Eur. J. Med. Chem. 58 , 171-83, (2012) A useful and rapid access to libraries of N-arylbenzo[b]thieno[3,2-d]pyrimidin-4-amines and their pyrido and pyrazino analogues was designed and optimized for the first time via microwave-accelerated condensation and Dimroth rearrangement of the starting anil... |
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Condensed heteroaromatic ring systems. XII. Synthesis of indole derivatives from ethyl 2-bromocarbanilates. Sakamoto T, et al.
Chem. Pharm. Bull. 35(5) , 1823-1828, (1987)
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Synthesis and Electronic Properties of 3-Acceptor-Substituted and 3, 7-Bisacceptor-Substituted Phenothiazines. Sailer M, et al.
European J. Org. Chem. 2006(2) , 423-435, (2006)
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