128961-19-3

Upstream product

• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 28448-83-1 2′-hydroxyl-4′-methoxyl-5′-isopentenylacetophenone 
• 128961-25-1 1-(4-methoxy-2-((3-methylbut-2-en-1-yl)oxy)phenyl)ethan-1-one 
• 123-08-0 4-hydroxy-benzaldehyde 

Downstream Products

• 129097-15-0 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one 

Relevant academic research and scientific papers

2-phenylchroman-4-one derivatives and antiviral composition comprising the same

The present invention relates to a 2-phenylchroman-4-one derivative or a pharmaceutically acceptable salt thereof, a method for manufacturing the same, and a therapeutic agent for MERS containing the same as an active component. A compound containing the

Method for synthesizing active ingredient intermediate of traditional Chinese medicine fructus psoraleae

The invention relates to a method for synthesizing an active ingredient intermediate of a traditional Chinese medicine fructus psoraleae. The method comprises the following steps: (a) mixing paeonol,1-bromo-3-methyl-2-butene and acetone, and adding potass

Synthesis method of active component of Chinese herb psoralea corylifolia

The invention relates to a synthesis method of an active component of a Chinese herb psoralea corylifolia. The synthesis method comprises the following steps: (a), mixing paeonol, 1-bromo-3-methyl-2-butene and acetone, adding potassium carbonate, and then

Separation and peroxisome proliferator-activated receptor-γ agonist activity evaluation of synthetic racemic bavachinin enantiomers

Abstract Bavachinin, isolated from Psoralea corylifolia seeds, has been reported to demonstrate peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist activity. However, isolated bavachinin is actually a mixture of S and R configurations, with an e

An Improved Procedure for Cyclisation of Chalcones to Flavanones Using Celite Supported Potassium Fluoride in Methanol: Total Synthesis of Bavachinin

Chalcones may be cyclised to the corresponding flavanones by stirring with KF - celite suspended in methanol at reflux.This method gives consistently higher conversion than other reported procedures and its utility is illustrated by the synthesis of the l