1088-08-0

Basic information

• Product Name: 2'',4'',6''-TRIHYDROXYDIHYDROCHALCONE
• Synonyms: Propiophenone,2',4',6'-trihydroxy-3-phenyl- (7CI,8CI); 2',4',6'-Trihydroxydihydrochalcone;2',4',6'-Trihydroxyhydrochalcone;3-Phenyl-1-(2,4,6-trihydroxyphenyl)-1-propanone
• CAS NO: 1088-08-0
• Molecular Formula: C₁₅H₁₄O₄
• Molecular Weight: 258.26926
• Product Categories: Chalcones
• Mol File: 1088-08-0.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2'',4'',6''-TRIHYDROXYDIHYDROCHALCONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2'',4'',6''-TRIHYDROXYDIHYDROCHALCONE(1088-08-0)
• EPA Substance Registry System: 2'',4'',6''-TRIHYDROXYDIHYDROCHALCONE(1088-08-0)

Safety Data

• Hazardous Substances Data: 1088-08-0(Hazardous Substances Data)

Usage

General Description

2'',4'',6''-Trihydroxydihydrochalcone is a chemical compound that belongs to the dihydrochalcone class. It is a natural sweetener found in various plants, including Stevia rebaudiana, and is known for its intense sweetness. 2'',4'',6''-TRIHYDROXYDIHYDROCHALCONE is commonly used as a sugar substitute in foods and beverages due to its low calorie content and strong sweetening properties. Additionally, 2'',4'',6''-Trihydroxydihydrochalcone has been studied for its potential therapeutic effects, including its antioxidant and anti-inflammatory properties, making it a subject of interest in the field of natural medicine and food science. Its versatile applications and potential health benefits make 2'',4'',6''-Trihydroxydihydrochalcone a widely researched and utilized chemical compound.

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 501-52-0 3-Phenylpropionic acid 
• 645-45-4 hydrocinnamic acid chloride 
• 524-14-1 S-(hydrogen malonyl)coenzyme A 
• 169132-91-6 (E)-1-(2-hydroxy-4,6-bis(methoxymethoxy)phenyl)-3-phenylprop-2-en-1-one 
• 65490-09-7 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone 
• 480-66-0 2,4,6-trihydroxyacetophenone 
• 100-52-7 benzaldehyde 
• 1122-91-4 4-bromo-benzaldehyde 
• 82451-30-7 2',4',6'-trihydroxychalcone 
• 128837-25-2 1-[2,4-bis(ethoxymethoxy)-6-hydroxyphenyl]ethan-1-one 
• 480-40-0 5,7-dihydroxy-2-phenyl-chromen-4-one 
• 102-93-2 3-phenylpropionamide 
• 645-59-0 dihydrocinnamonitrile 

Downstream Products

• 135383-81-2 3′-formyl-2′,4′,6′-trihydroxydihydrochalcone 
• 10499-26-0 grandiflorone 
• 1266170-07-3 1-[3-(β-D-glucopyranosyl)-2,4,6-trihydroxyphenyl]-3-phenylpropan-1-one 
• 906433-07-6 (+/-) linderatin 
• 34328-57-9 2,2,4-trimethyl-6-(1-oxo-3-phenylpropyl)cyclohexane-1,3,5-trione 
• 1235289-00-5 2',4',6'-trihydroxy-3',5'-di-C-β-D-glucopyranosyldihydrochalcone 
• 70155-33-8 1-(2,4,6-trihydroxy-3-methyl)phenyl-3-phenyl-1-propanone 
• 50861-53-5 2,2,4,4-tetramethyl-6-(3'-phenylpropionyl)cyclohexane-1,3,5-trione 
• 120217-41-6 neolinderachalcone 

Relevant articles and documents

Hydrogen-bonded rotamers of 2′,4′,6′-trihydroxy-3′-formyldihydrochalcone, an intermediate in the synthesis of a dihydrochalcone from Leptospermum recurvum

Synthesis of 2′,4′,6′-trihydroxy-3′-methyldihydrochalcone, isolated as a natural product for the first time (ex Leptospermum recurvum), proceeds through 2′,4′,6′-trihydroxy-3′-formyldihydrochalcone. Two stable rotamers of this formyl derivative have been

DIHYDROCHALCONES FROM LINDERA UMBELLATA

Two dihydrochalcones, 2',6'-dihydroxy-4'-methoxydihydrochalcone and 2',4',6'-trihydroxydihydrochalcone have been isolated form leaves of Lindera umbellata.Key words: Lindera umbellata; Lauraceae; 2',6'-dihydroxy-4'-methoxydihydrochalcone; 2',4',6'-trihydr

Quinoid dihydrochalcone dicarbonyl glycoside compound with glucose on A ring, preparation method and neuroprotective activity thereof

The invention discloses a class of quinoid dihydrochalcone C-glycoside compounds with glucose on a ring A, a preparation method and anti-cerebral ischemia injury activity thereof, wherein the compoundhas a structure represented by a general formula (I). The preparation method of the compound comprises the following steps: (1) synthesizing a 2,4,6-trihydroxy dihydrochalcone compound; (2) synthesizing a 2,4,6-trihydroxy-3,5-diglucosyl dihydrochalcone C-glycoside compound; and (6) synthesizing a class of quinoid dihydrochalcone C-glycoside compound with glucose in the A ring. The compound disclosed by the invention is simple in preparation method and has a remarkable effect of resisting cerebral ischemia injury.

Base-catalyzed oxidative dearomatization of multisubstituted phloroglucinols: An easy access to C-glucosyl 3,5,6-trihydroxycyclohexa-2,4-dienone derivatives

An efficient and simple method for the protecting group-free synthesis of C-glucosyl 3,5,6-trihydroxycyclohexa-2,4-dienone has been firstly established. This method is compatible with various functional groups, such as benzyl and phenethyl groups, affording a range of C-glucosyl 3,5,6-trihydroxycyclohexa-2,4-dienone derivatives.