ChemicalBook--->CAS DataBase List--->13425-93-9

13425-93-9

13425-93-9 Structure

13425-93-9 Structure
IdentificationMore
[Name]

4-Hydroxy-6,7-dimethoxyqunioline
[CAS]

13425-93-9
[Synonyms]

4-HYDROXY-6,7-DIMETHOXYQUINOLINE
6,7-DIMETHOXYQUINOLIN-4(1H)-ONE
4-HYDROXY-6,7-DIMETHOXYQUNIOLINE
6,7-Dimethoxy-quinolin-4-ol
[EINECS(EC#)]

811-007-0
[Molecular Formula]

C11H11NO3
[MDL Number]

MFCD07368026
[Molecular Weight]

205.21
[MOL File]

13425-93-9.mol
Questions And AnswerBack Directory
[Appearance]

4-Hydroxy-6,7-dimethoxyqunioline is a slightly pale yellow to yellow solid.
Chemical PropertiesBack Directory
[Melting point ]

227.0 to 231.0 °C
[Boiling point ]

370.9±37.0 °C(Predicted)
[density ]

1.257±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

DMSO (Slightly), Methanol (Slightly, Sonicated)
[form ]

powder to crystal
[pka]

4.26±0.40(Predicted)
[color ]

Light orange to Yellow to Green
[InChI]

InChI=1S/C11H11NO3/c1-14-10-5-7-8(6-11(10)15-2)12-4-3-9(7)13/h3-6H,1-2H3,(H,12,13)
[InChIKey]

QOGPNCUTXVZQSL-UHFFFAOYSA-N
[SMILES]

N1C2C(=CC(OC)=C(OC)C=2)C(O)=CC=1
[CAS DataBase Reference]

13425-93-9(CAS DataBase Reference)
Safety DataBack Directory
[HS Code ]

2933.49.7000
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Uses]

6,7-Dimethoxy-4-quinolinol was used in the study of synthesis of ring-substituted 4-aminoquinolines and evaluation fo their antimalarial activities.
[Synthesis]

ethyl 4-hydroxy-6,7-dimethoxyquinoline-3-carboxylate

13436-14-1

4-Hydroxy-6,7-dimethoxyqunioline

13425-93-9

General procedure for the synthesis of 4-hydroxy-6,7-dimethoxyquinoline-3-carboxylic acid from ethyl 4-hydroxy-6,7-dimethoxyquinoline-3-carboxylate: ethyl 4-hydroxy-6,7-dimethoxyquinoline-3-carboxylate (700 mg, 2.53 mmol) was added to potassium hydroxide (450 mg, 7.6 mmol) dissolved in 20 mL of H2O/EtOH (1:1, v /v) solution. The mixture was placed in a sealed container (XP-500 Plus container) and heated using microwaves (MARS 5 Microwave System) at 180°C, 260-280 psi pressure for 50 min. Upon completion of the reaction, the mixture was cooled to room temperature and transferred to a flask. Subsequently, the solution was acidified to pH about 6 with acetic acid (about 2 mL), saturated with sodium chloride, and extracted with tetrahydrofuran (3 x 100 mL). The organic layers were combined, washed with brine and concentrated to give 6,7-dimethoxyquinolin-4-ol in 90% yield.1H NMR (400 MHz, DMSO-d6) δ ppm: 3.81 (s, 3H), 3.84 (s, 3H), 5.93 (d, J=7.3 Hz, 1H), 7.05 (s, 1H), 7.42 (s, 1H), and 7.76 (d, J=7.3 Hz, 1H).

[storage]

Store at room temperature.
[References]

[1] Patent: WO2005/121125, 2005, A1. Location in patent: Page/Page column 41-42
[2] Journal of the American Chemical Society, 1946, vol. 68, p. 1264
Spectrum DetailBack Directory
[Spectrum Detail]

4-Hydroxy-6,7-dimethoxyqunioline(13425-93-9)1HNMR
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