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CasNo： 574-12-9
MF： C15H10O2
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Isoflavones possess antioxidant properties and antipromotional effects.
3-bromo-4H-chromen-4-one
phenylboronic acid
isoflavone
| Conditions | Yield |
|---|---|
|
With
sodium carbonate;
tetrakis(triphenylphosphine) palladium(0);
In
water; benzene;
for 6h;
Heating;
|
94% |
|
With
tetrakis(triphenylphosphine) palladium(0); sodium carbonate;
In
benzene;
for 53h;
Reflux;
Inert atmosphere;
|
94% |
|
With
potassium carbonate;
(1-benzothiazol-2-yl-ethanone oxime)dichloropalladium(II);
In
toluene;
at 150 ℃;
for 0.133333h;
microwave irradiation;
|
93% |
|
With
tetrabutylammomium bromide; sodium carbonate;
In
water;
at 100 ℃;
for 1h;
Solvent;
Concentration;
Green chemistry;
|
93% |
|
With
dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; potassium carbonate;
In
water; N,N-dimethyl-formamide;
at 90 ℃;
Inert atmosphere;
|
86% |
|
With
sodium carbonate;
tetrakis(triphenylphosphine) palladium(0);
In
water; benzene;
for 6h;
Product distribution;
Heating;
other bases and reaction time;
|
|
|
With
potassium carbonate;
trans-[PdCl2(2-ethyl-2-oxazoline-κ1N)2];
In
toluene;
for 24h;
Heating;
|
|
|
With
tetrakis(triphenylphosphine) palladium(0); sodium carbonate;
In
toluene;
Inert atmosphere;
Reflux;
|
salicylaldehyde
α-bromoacetophenone
isoflavone
| Conditions | Yield |
|---|---|
|
α-bromoacetophenone;
With
thiamine hydrochloride;
In
ethanol;
at 20 ℃;
for 0.25h;
Green chemistry;
salicylaldehyde;
In
ethanol;
at 20 ℃;
for 1h;
Solvent;
Time;
Reagent/catalyst;
Green chemistry;
|
88% |
The CAS number of Isoflavone is 574-12-9.
More information of Isoflavone 574-12-9 are:
|
CAS Number |
574-12-9 |
|
Density |
1.239 g/cm3 |
|
Melting Point |
150oC |
|
Boiling Point |
367 °C at 760 mmHg |
|
Flash Point |
171.1 °C |
|
Vapor Pressure |
1.41E-05mmHg at 25°C |
|
Refractive Index |
1.6600 (estimate) |
|
HS CODE |
2914399090 |
|
PSA |
30.21000 |
|
LogP |
3.46000 |
Synonyms for Isoflavone 574-12-9:Isoflavone(6CI,7CI,8CI);3-Phenyl-4-chromone;3-Phenylchromone;Isoflavone 80;NSC 135405;4H-1-Benzopyran-4-one,3-phenyl-;
The chemical formula of Isoflavone is C15H10O2 which containing 15 Carbon atoms,10 Hydrogen atoms and 2 Oxygen atoms,and the molecular weight of Isoflavone is 222.243.
Isoflavone is a naturally occurring compound belonging to the class of isoflavones, characterized by its 4H-chromen-4-one structure with a phenyl group replacing the hydrogen at position 3. It is known for its antioxidant properties, estrogen-like effects, and various health benefits.
InChI:InChI=1/C15H10O2/c16-15-12-8-4-5-9-14(12)17-10-13(15)11-6-2-1-3-7-11/h1-10H
Relevant articles related to Isoflavone:
|
Article |
Source |
|
Identification of ortho catechol-containing isoflavone as a privileged scaffold that directly prevents the aggregation of both amyloid β plaques and tau-mediated neurofibrillary tangles and its in vivo evaluation |
Do, Ji Min,Gee, Min Sung,Inn, Kyung-Soo,Kim, Jong-Ho,Kim, Nam Kwon,Kim, Nam-Jung,Lee, Hyun Woo,Lee, Jong Kil,Seo, Min-Duk,Seong, Ji Hye,Son, Seung Hwan,Yoo, Hyung-Seok,Yoo, Ji-Na , (2021/07/01) |
|
Ionic liquids and ohmic heating in combination for Pd-catalyzed cross-coupling reactions: Sustainable synthesis of flavonoids |
Silva, Artur M. S.,Silva, Vera L. M.,Soengas, Raquel G. , (2020/04/09) |
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