4-Hydroxy-1-Methyl-2-quinolone
4-Hydroxy-1-Methyl-2-quinolone structure
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Common Name | 4-Hydroxy-1-Methyl-2-quinolone | ||
|---|---|---|---|---|
| CAS Number | 1677-46-9 | Molecular Weight | 175.184 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 297.6±40.0 °C at 760 mmHg | |
| Molecular Formula | C10H9NO2 | Melting Point | 269-271 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 133.8±27.3 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Over-expression of bael quinolone synthase in tobacco improves plant vigor under favorable conditions, drought, or salt stress.
FEBS Lett. 589(3) , 332-41, (2015) Type III polyketide synthases (PKSs) catalyze the biosynthesis of various medicinally important secondary metabolites in plants, but their role in growth and stress response is unclear. Here, we overexpressed quinolone synthase (QNS) from bael in tobacco. QNS... |
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Mechanistic study of electrochemical oxidation of catechols in the presence of 4-hydroxy-1-methyl-2 (1H)-quinolone: Application to the electrochemical synthesis. Fakhari AR, et al.
Electrochim. Acta 50(27) , 5322-5328, (2005)
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Ceric ammonium nitrate (CAN)-mediated oxidative cycloaddition of 1, 3-dicarbonyls to conjugated compounds. Efficient synthesis of dihydrofurans, dihydrofurocoumarins, dihydrofuroquinolinones, dihydrofurophenalenones, and furonaphthoquinone natural products. Lee YR, et al.
Tetrahedron 56(45) , 8845-53, (2000)
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Iridium catalysed alkylation of 4-hydroxy coumarin, 4-hydroxy-2-quinolones and quinolin-4 (1H)-one with alcohols under solvent free thermal conditions. Grigg R, et al.
Tetrahedron 65(36) , 7468-7473, (2009)
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