4-Hydroxy-1-Methyl-2-quinolone

Modify Date: 2024-01-02 10:12:53

4-Hydroxy-1-Methyl-2-quinolone Structure
4-Hydroxy-1-Methyl-2-quinolone structure
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
GHS07
Signal Word Warning

 Names

Name 4-hydroxy-1-methylquinolin-2-one
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.3±0.1 g/cm3
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

 Safety Information

Symbol GHS07
GHS07
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

 Synthetic Route

 Customs

HS Code 2933790090
Summary 2933790090. other lactams. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:9.0%. General tariff:20.0%

 Articles4

More Articles
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...

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)

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)

 Synonyms

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-