5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE
5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE Basic information
- Product Name:
- 5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE
- Synonyms:
-
- 5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE
- 5-Methoxy-1,2,3,4-tetrahydroisoquinolin-1-one
- 5-Methoxy-3,4-dihydro-2H-isoquinolin-1-one
- 5-Methoxy-3,4-dihydroisoquinolin-1(2H)
- 1(2H)-Isoquinolinone, 3,4-dihydro-5-methoxy-
- CAS:
- 129075-49-6
- MF:
- C10H11NO2
- MW:
- 177.2
- Mol File:
- 129075-49-6.mol
5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to off-white Solid
5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE Usage And Synthesis
Synthesis
13336-31-7
129075-49-6
GENERAL METHOD: 4-methoxy-1-indanone (1.5 mmol) was dissolved in 37% hydrochloric acid (5 mL) at 0°C and sodium azide (NaN3, 0.2 g, 3.0 mmol) was added slowly. The reaction mixture was stirred at room temperature overnight. Upon completion of the reaction, the mixture was poured into ice water and adjusted to alkaline with sodium carbonate (Na2CO3). The aqueous phase was extracted with ethyl acetate (3 x 10 mL). The organic phases were combined, dried with anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to give the crude product. The crude product was purified by column chromatography with the eluent being a solvent mixture of dichloromethane (CH2Cl2) and ethyl acetate (AcOEt) (9:1, v/v).
References
[1] European Journal of Medicinal Chemistry, 2013, vol. 69, p. 920 - 930
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5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE(129075-49-6)Related Product Information
- 5-METHOXY-1,2,3,4-TETRAHYDRO-QUINOLINE HYDROCHLORIDE
- 5-Methoxy-1,2,3,4-tetrahydroquinoline hydrochloride
- 5-Chloro-3-methylpyridine-2-carbonitrile
- 5-BROMO-1H-PYRAZOLE-3-CARBALDEHYDE
- 5-FLUORO-1H-BENZIMIDAZOLE
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- AKOS 214-22
- AKOS 214-58
- AKOS 237-34
- DPQ
- 5-(3-CHLORO-PROPOXY)-3,4-DIHYDRO-2H-ISOQUINOLIN-1-ONE
- 5-METHOXY-3,4-DIHYDRO-1(2H)-ISOQUINOLINONE