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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
1022-66-8

3-PHENYL-3,4-DIHYDROQUINOLIN-2(1H)-ONE synthesis

7synthesis methods
Benzeneacetic acid, α-[(2-nitrophenyl)methylene]-, (αE)-

19319-35-8
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3-PHENYL-3,4-DIHYDROQUINOLIN-2(1H)-ONE

1022-66-8
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-

Yield:1022-66-8 85%

Reaction Conditions:

with hydrogen;palladium on activated charcoal in methanol; for 6 h;Ambient temperature;

References:

Hino;Nagai;Uno [Chemical and Pharmaceutical Bulletin,1987,vol. 35,# 7,p. 2819 - 2824]

201230-82-2 Synthesis
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3-PHENYL-3,4-DIHYDROQUINOLIN-2(1H)-ONE

1022-66-8
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References
3900-89-8 Synthesis
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3-PHENYL-3,4-DIHYDROQUINOLIN-2(1H)-ONE

1022-66-8
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3-PHENYL-3,4-DIHYDROQUINOLIN-2(1H)-ONE

1022-66-8
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3-PHENYL-3,4-DIHYDROQUINOLIN-2(1H)-ONE

1022-66-8
10 suppliers
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References