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Reputable factory supply PRUNINDIHYDROCHALCONE 4192-90-9 in bulk at low price
- Molecular Formula: C21H24O10
- Molecular Weight: 436.416
- Vapor Pressure: 3.71E-26mmHg at 25°C
- Melting Point: 170-173 °C
- Boiling Point: 787.9°Cat760mmHg
- PKA: 6.85±0.40(Predicted)
- Flash Point: 277.1°C
- PSA: 177.14000
- Density: 1.555g/cm3
- LogP: -0.20240
PRUNINDIHYDROCHALCONE(Cas 4192-90-9) Usage
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General Description |
Prunindihydrochalcone is a chemical compound found in the leaves of Prunus Mume (also known as Chinese Plum or Japanese Apricot) and is known for its potential sweetening properties. It is a type of dihydrochalcone, which is a class of natural sweeteners that are derived from plants. Prunindihydrochalcone has been studied for its potential as a low-calorie sweetener and has been found to have a sweet taste without the potential negative health effects associated with traditional sugar. It is also being researched for its potential use in the food and beverage industry as a natural and safe alternative to artificial sweeteners. |
InChI:InChI=1/C21H24O10/c22-9-16-18(27)19(28)20(29)21(31-16)30-12-7-14(25)17(15(26)8-12)13(24)6-3-10-1-4-11(23)5-2-10/h1-2,4-5,7-8,16,18-23,25-29H,3,6,9H2/t16-,18-,19+,20-,21-/m1/s1
4192-90-9 Relevant articles
Synthesis of trilobatin from naringin via prunin as the key intermediate: Acidic hydrolysis of the α-rhamnosidic linkage in naringin under improved conditions
Kurahayashi, Kazuki,Hanaya, Kengo,Higashibayashi, Shuhei,Sugai, Takeshi
, p. 1463 - 1467 (2018/09/13)
Trilobatin [4-(β-D-glucopyranosyloxy)-2,...
Exploring the catalytic promiscuity of a new glycosyltransferase from Carthamus tinctorius
Xie, Kebo,Ridao, Chen,Li, Jianhua,Wang, Ruishan,Chen, Dawei,Dou, Xiaoxiang,Dai, Jungui
supporting information, p. 4874 - 4877 (2015/04/27)
The catalytic promiscuity of a new glyco...
Synthesis and biological evaluation of phloridzin analogs as human concentrative nucleoside transporter 3 (hCNT3) inhibitors
Gupte, Amol,Buolamwini, John K.
supporting information; experimental part, p. 917 - 921 (2009/09/06)
Nucleoside transporter inhibitors have p...
4192-90-9 Process route
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4'-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)-2',4”,6'-tribenzyloxychalcone
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4192-90-9
4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone
| Conditions | Yield |
|---|---|
|
With
10 wt% Pd(OH)2 on carbon; hydrogen;
In
methanol; ethyl acetate;
at 20 ℃;
for 19h;
|
93%
|
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1133352-99-4
C29 H32 O14
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4192-90-9
4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone
| Conditions | Yield |
|---|---|
|
With
sodium methylate;
In
methanol;
for 5h;
Reflux;
|
50%
|
4192-90-9 Upstream products
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18916-17-1
[4-[[2-O-(6-deoxy-L-mannopyranosyl)-D-glucopyranosyl]oxy]-2,6-dihydroxyphenyl]-3-(4-hydroxyphenyl)-1-propanone
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10236-47-2
naringin
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50376-43-7
4'-rhamnoglucosyloxy-2',4,6'-trihydroxychalcone
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1133352-99-4
C29 H32 O14
4192-90-9 Downstream products
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60-82-2
3-(4-Hydroxy-phenyl)-1-(2,4,6-trihydroxy-phenyl)-propan-1-on
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