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CasNo: 1214-47-7
MF: C15H12O2
Appearance: luidity powder
Preparation |
Synthesis of 2'-hydroxychalcone: add 30 ml of 20% (V/V) ethanol and (11.06 mmol) sodium hydroxide in a 50 mL single mouth flask, stir for 0.5 h at room temperature and then add substituted 2-Hydroxyacetophenone (1.66 mmol) and benzaldehyde (1.66 mmol), stir for 18 h at room temperature, TLC monitoring until the new point produces raw material point no longer changes, stop the reaction Then the reaction was poured into water, stirred while adjusting the pH value to acidic with 6 mol/L hydrochloric acid, the reaction was filtered, the filter cake was obtained, rinsed twice with pure water, and 2'-hydroxychalcone was obtained by silica gel column chromatography [V(petroleum ether):V(ethyl acetate) = 5:1] in 85% yield. |
Definition |
ChEBI: 2'-hydroxychalcone is a member of the class of chalcones that is trans-chalcone substituted by a hydroxy group at position 2'. It has a role as an anti-inflammatory agent. It is a member of phenols and a member of chalcones. It derives from a trans-chalcone. |
InChI:InChI=1/C15H12O2/c16-14-9-5-4-8-13(14)15(17)11-10-12-6-2-1-3-7-12/h1-11,16H/b11-10+
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phenyl cinnamate
4'-hydroxychalcone
1-(2-hydroxyphenyl)-3-phenylprop-2-en-1-one
Conditions | Yield |
---|---|
With sodium dodecyl-sulfate; for 7h; Irradiation;
|
15% 70% |
salicylaldehyde
phenylacetylene
FLAVONE
1-(2-hydroxyphenyl)-3-phenylprop-2-en-1-one
Conditions | Yield |
---|---|
With piperidine; iron(III) chloride; In toluene; for 8h; Reflux;
|
80% 4% |
phenyl cinnamate
2'-hydroxychalcone dibromides
o-hydroxyacetophenone
benzaldehyde
cis-4-hydroxyflavan
1-(2-hydroxy-phenyl)-4-(3-methyl-4-nitro-isoxazol-5-yl)-3-phenyl-butan-1-one
(2-Hydroxy-phenyl)-(4-phenyl-4,5-dihydro-1H-pyrazol-3-yl)-methanone
1-(o-Hydroxyphenyl)-3-phenyl-3-(2'-oxocyclohexyl)-1-propanone