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ChemicalBook--->CAS DataBase List--->190728-25-7

190728-25-7

190728-25-7 Structure

190728-25-7 Structure
IdentificationBack Directory
[Name]

BenzenaMine, 4-[(6,7-diMethoxy-4-quinolinyl)oxy]-
[CAS]

190728-25-7
[Synonyms]

4-(6,7-Dimethoxy-quinoL
Intermediate 1 of Cabozantinib
Cabozantinib Genotoxic Impurity I
4-[(6,7-dimethoxy-4-quinolinyl)oxy]-
4-(6,7-dimethoxy quinolinoxy) aniline
4-(4-Aminophenoxy)-6,7-dimethoxyquinoline
6,7-Dimethoxy-4-(4-aminophenoxy)quinoline
4-[(6,7-Dimethoxyquinolin-4-yl)oxy]aniline
6,7-Dimethoxy-4-(4-aminophenyloxy)quinolone
4-(2,3-dimethoxynaphthalen-5-yloxy)benzenamine
BenzeMine, 4-[(6,7-diMethoxy-4-quinolinyl)oxy]-
4-[(6,7-diMethoxy-4-quinolinyl)oxy]-BenzenaMine
[4-[(6,7-Dimethoxyquinolin-4-yl)oxy]phenyl]amine
BenzenaMine, 4-[(6,7-diMethoxy-4-quinolinyl)oxy]-
4-[(6,7-dimethoxyquinolin-4-yl)oxy]aniline 4-((6,7-Dimethoxyquinolin-4-yl)oxy)aniline
[Molecular Formula]

C17H16N2O3
[MDL Number]

MFCD19685633
[MOL File]

190728-25-7.mol
[Molecular Weight]

296.321
Chemical PropertiesBack Directory
[Melting point ]

211.0 to 215.0 °C
[Boiling point ]

481.8±45.0 °C(Predicted)
[density ]

1.246±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[solubility ]

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

powder to crystal
[pka]

6.79±0.30(Predicted)
[color ]

Light yellow to Brown
[InChI]

InChI=1S/C17H16N2O3/c1-20-16-9-13-14(10-17(16)21-2)19-8-7-15(13)22-12-5-3-11(18)4-6-12/h3-10H,18H2,1-2H3
[InChIKey]

VXEQRXJATQUJSN-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=C(OC2C3C(N=CC=2)=CC(OC)=C(OC)C=3)C=C1
Safety DataBack Directory
[HS Code ]

2933.49.7000
Hazard InformationBack Directory
[Uses]

4-(6,7-Dimethoxy-Quinolin-4-Yloxy)-Phenylamine is used in preparation of Cabozantinib Defluorination impurity.
[Chemical Reactivity]

4-((6,7-Dimethoxyquinolin-4-yl)oxy)aniline is a primary alcohol that has been shown to catalyze the reaction of potassium carbonate with an alkali metal hydroxide to produce potassium. It has also been shown to be a base catalyst for the reaction of cyclopropanecarboxylic acid with an alcohol ester to produce high yield.
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