4-Hydroxy-1-Methyl-2-quinolone structure
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Common Name | 4-Hydroxy-1-Methyl-2-quinolone | ||
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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 |
Name | 4-hydroxy-1-methylquinolin-2-one |
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Synonym | More Synonyms |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 297.6±40.0 °C at 760 mmHg |
Melting Point | 269-271 °C(lit.) |
Molecular Formula | C10H9NO2 |
Molecular Weight | 175.184 |
Flash Point | 133.8±27.3 °C |
Exact Mass | 175.063324 |
PSA | 42.23000 |
LogP | 1.31 |
Vapour Pressure | 0.0±0.7 mmHg at 25°C |
Index of Refraction | 1.647 |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xi: Irritant; |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
RTECS | FG7350000 |
HS Code | 2933790090 |
Precursor 9 | |
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DownStream 10 | |
HS Code | 2933790090 |
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Summary | 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0% |
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 overe... |
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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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4-hydroxy-1-methyl-1,2-dihydro-2-quinolinone |
1-methyl-4-hydroxy-2(1H)-quinolinone |
4-Hydroxy-1-methyl-2-quinolone |
4-Hydroxy-1-methyl-2(1H)-quinolinone |
4-Hydroxy-N-methylcarbostyril |
N-methyl-4-hydroxyquinolin-2(1H)-one |
EINECS 216-830-3 |
1-methyl-4-hydroxyquinolin-2(1H)-one |
4-Hydroxy-1-methyl-2(1H)-quinolone |
4-hydroxy-1-methylquinolin-2(1H)-one |
4-hydroxy-1-methyl-2-quinolinone |
4-Hydroxy-1-methylcarbostyril |
2(1H)-Quinolinone,4-hydroxy-1-methyl |
1-Methyl-4-hydroxycarbostyril |
CARBOSTYRIL,4-HYDROXY-1-METHYL |
4-Hydroxy-1-methyl-1H-quinolin-2-one |
MFCD00024052 |
1,2-dihydro-4-hydroxy-N-methylquinolin-2-one |
2(1H)-Quinolinone, 4-hydroxy-1-methyl- |