Catalyst and Auxiliary

4192-90-9

  • Product Name：PRUNINDIHYDROCHALCONE
  • Molecular Formula：C21H24O10
  • Specifications：99%
  • Molecular Weight：436.416
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Product Details;

CasNo： 4192-90-9

Molecular Formula： C21H24O10

Chinese Manufacturer supply PRUNINDIHYDROCHALCONE 4192-90-9 in stock with high standard

  • 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

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

4'-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)-2',4”,6'-tribenzyloxychalcone

4'-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyloxy)-2',4”,6'-tribenzyloxychalcone

4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone
4192-90-9

4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone

Conditions
Conditions Yield
With 10 wt% Pd(OH)2 on carbon; hydrogen; In methanol; ethyl acetate; at 20 ℃; for 19h;
93%
C<sub>29</sub>H<sub>32</sub>O<sub>14</sub>
1133352-99-4

C29H32O14

4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone
4192-90-9

4'-(β-D-glucopyranosyloxy)-2',4”,6'-trihydroxydihydrochalcone

Conditions
Conditions Yield
With sodium methylate; In methanol; for 5h; Reflux;
50%

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4192-90-9 Downstream products

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    3-(4-Hydroxy-phenyl)-1-(2,4,6-trihydroxy-phenyl)-propan-1-on

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